Macrophages/Monocytes Antibody | MOMA-2

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Macrophages/Monocytes Antibody | MOMA-2 gallery image 1

Staining of mouse peritoneal macrophages with FITC conjugated Rat anti Mouse Macrophages/Monocytes (MCA519FA) following permeabilisation with Leucoperm (BUF09)

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Staining of mouse peritoneal macrophages with RPE conjugated Rat anti Mouse Macrophages/Monocytes (MCA519PE) following permeabilisation with Leucoperm (BUF09)

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Rat anti Mouse Macrophages/Monocytes antibody, clone MOMA-2 used for the detection of macrophages in atherosclerotic aotic lesions from control and ApoE knockout mice.
Image caption:
MOMA-2 staining of ApoE-/- (SKO) and ApoE-/-, P-selectin-/- (DKO) mice fed a chow diet. Macrophages, stained by MOMA-2 monoclonal antibody, are shown binding the endothelial layer and penetrating the intimal lesions in SKO (a, c) and DKO (b, d) animals following, respectively, 15- (a, b) and 20- (c, d) week chow diet. Black arrows show immunostained macrophages. Original magnification: x250.

From: Marie-Claude Bourdillon, Jacques Randon, Lydie Barek, et al., “Reduced Atherosclerotic Lesion Size in -Selectin Deficient Apolipoprotein -Knockout Mice Fed a Chow but Not a Fat Diet ,”
Journal of Biomedicine and Biotechnology, vol. 2006, Article ID 49193, 8 pages, 2006.

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Rat anti Mouse Macrophages/Monocytes antibody, clone MOMA-2 used for the detection of macrophages in adipose tissue of mice using immunohistochemistry.
Image caption:
High number of preadipocyte/macrophage-like cells in the adipose tissue of Nscl-2 (-/-) and Nscl-2 (-/-)×ob/ob compound mutant mice. (A) Number of preadipocyte/macrophage-like cells per 250 adipocytes (F = 250.71; dF = 3; p<10-4; 4 mice per group). (B) Number of MOMA-2 positive but F4/80 negative cells per 250 adipocytes. The difference between MOMA-2 and F4/80 positive cells corresponds to adipocyte precursors (p = 0.038). (C) Richardson-stain of a section of epididymal adipose tissue from 6 months old male double mutant mouse. Arrow indicates groups of preadipocyte/macrophage-like cells between fat cells (scale bar: 25 µm). (D) MOMA-2 staining of paraffin embedded epididymal adipose tissue of a Nscl-2 (-/-) mouse (scale bar: 100 µm). The inlet shows a typical staining of MOMA-2 (scale bar: 15 µm).

From: Ruschke K, Ebelt H, Klöting N, Boettger T, Raum K, Blüher M, et al. (2009) Defective Peripheral Nerve Development Is Linked to Abnormal Architecture and Metabolic Activity of Adipose Tissue in Nscl-2 Mutant Mice.
PLoS ONE 4(5): e5516.

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Rat anti Mouse Macrophages/Monocytes antibody, clone MOMA-2 used for the detection of macrophages in mouse liver by immunofluorescence on formalin fixed tissue sections.
Image caption:
S. Typhimurium Reside in Macrophages That Appear to Have Multiple Nuclei Confocal fluorescence microscopy of 50-μm-thick liver sections from a 1-wk-infected Slc11a1 (Nramp1) wild-type mouse. S. Typhimurium (O-antigen, arrows) are red, macrophages (F4–80 and MOMA-2) are blue, DNA (DAPI) is gray, and phalloidin is green. (A) Low power image, scale bar is 40 μm. (B–H) Montage of 4-μm optical sections through the boxed region of (A). Scale bar is 20 μm. (I and J) Enlarged images showing actin rings (arrowheads) around nuclei within the multinucleate macrophage. The endogenous macrophage nucleus is visible in (I) and is labeled with an N.

From: Nix RN, Altschuler SE, Henson PM, Detweiler CS (2007) Hemophagocytic Macrophages Harbor Salmonella enterica during Persistent Infection.
PLoS Pathog 3(12): e193.

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Rat anti Mouse Macrophages/Monocytes antibody, clone MOMA-2 used for the detection of macrophages in mouse liver by immunofluorescence on formalin fixed tissue sections.
Image caption:
S. Typhimurium-Infected Macrophages Containing Phagocytosed Neutrophils and T Cells Confocal fluorescence microscopy of 50-μm-thick liver sections from 1-wk-infected Slc11a1 wild-type mice. (A–C) S. Typhimurium (O-antigen, arrows) are red, macrophages (F4–80 and MOMA-2) are blue, DNA (DAPI) is gray, phalloidin is green, and neutrophils (Gr-1/Ly-6G/RB6-8C5) are pink (arrowheads). (A) Collapsed image from a 40-μm Z-stack. Scale bar is 20 µm. (B and C) Sections from (A) that are 4 μm apart. (D–G) T cells within multinucleate macrophages. Macrophages (F4–80 and MOMA-2) are blue (D, G, and H), T cells (CD3zeta) are red (D, G, arrowheads), DAPI is gray (E, G), actin-bound phalloidin is green (F, G). (G) Is a composite of (D, E, and F). Scale bars are 16 μm. (H) An image from a different mouse stained and labeled as described for (D–G). Scale bar is 8 µm.

From: Nix RN, Altschuler SE, Henson PM, Detweiler CS (2007) Hemophagocytic Macrophages Harbor Salmonella enterica during Persistent Infection.
PLoS Pathog 3(12): e193.

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Rat anti Mouse Macrophages/Monocytes antibody, clone MOMA-2 used for the detection of bone marrow derived macrophages in mouse by immunofluorescence.
Image caption:
ctivated Bone Marrow–Derived Macrophages (BMDMs) Phagocytose Live Host Cells Confocal fluorescence microscopy. BMDMs are blue (F4–80 and MOMA-2), human T cells (Jurkats) are green (CMFDA-stained), and DNA is gray (DAPI). (A–C) 30 min after the addition of Jurkats to BMDMs. (A) Unactivated BMDMs show little association with Jurkat cells, many of which were washed away. Scale bar is 40 μm (B and C). Activated macrophages phagocytose Jurkat cells; arrow denotes engulfed cell, arrowheads show partially engulfed cells. Scale bars are 40 μm (B) and 8 μm (C). (D–F) 42 h after mock-infection (D), or S. Typhimurium-infection (O-antigen, red, arrows, E and F). Scale bars are 20 µm (D), 40 µm (E), and 16 µm (F)..

From: Nix RN, Altschuler SE, Henson PM, Detweiler CS (2007) Hemophagocytic Macrophages Harbor Salmonella enterica during Persistent Infection.
PLoS Pathog 3(12): e193.

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Rat anti Mouse Macrophages/Monocytes antibody, clone MOMA-2 used for the detection of macrophages in aortic atherosclerotic lesions by immunohistochemistry on cryosections.
Image caption:
Representative sections with immunohistochemical analysis. Apo E-knockout mice were fed a Western-type diet and treated with PBS (control group) (n = 10) or 1 mg/kg/day 15d-PGJ2 (15d-PGJ2 group) (n = 10) for 2 mo. Representative cross-sections of the aortic sinus were stained with MOMA-2 (A), which detected macrophages, and MCP-1 Abs (B), MIF Abs (C), TNF-a Abs (D), MMP-9 Abs (E), PPARγ Abs (F), and counterstained with hematoxylin. Right sections are control group and left ones are 15d-PGJ2 group in each figure. Black arrows indicate the positive lesions.

From: Seno T, Hamaguchi M, Ashihara E, Kohno M, Ishino H, Yamamoto A, et al. (2011) 15-Deoxy-Δ12,14 Prostaglandin J2 Reduces the Formation of Atherosclerotic Lesions in Apolipoprotein E Knockout Mice. PLoS ONE 6(10): e25541.

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Rat anti Mouse Macrophages/Monocytes antibody, clone MOMA-2 used to immunostain RAW 264.7 cells using immunofluorescence.
Image caption:
Immunofluorescence and western blot analysis of MMP-2 and MMP-9 expression in vitro. Panel A shows the immunofluorescence images of MMP-2 in macrophages receiving doxycycline, simvastatin or no treatment. Panel B shows the immunofluorescence images of MMP-9 in macrophages receiving doxycycline, simvastatin or no treatment. Panel C shows western blot analysis of MMP-2 and MMP-9 expression. Panel D and E are the quantitative analysis of Panel C. Blue color represents DAPI staining, green color MOMA-2 staining and red color MMP-2 or MMP-9 staining. Bars = 20 μm. Group D: doxycycline-treated group; Group S: simvastatin-treated group; Control: control group. **P<0.01, vs. Control group.

From: Dong M, Zhong L, Chen WQ, Ji XP, Zhang M, Zhao YX, et al. (2012) Doxycycline Stabilizes Vulnerable Plaque via Inhibiting Matrix Metalloproteinases and Attenuating Inflammation in Rabbits.
PLoS ONE 7(6): e39695.

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Rat anti Mouse Macrophages/Monocytes antibody, clone MOMA-2 used for the demonstation of macrophages in aortic atherosclerotic lesions by immunohistochemistry on cryosections.
Image caption:
p210 immunization confers protection against atherosclerosis. Representative pictures of aortic en-face lipid staining from each group shown (A; left panel). Immunization with native p210 resulted in a significant reduction in aortic atherosclerosis when compared to PBS and cBSA/Alum group (A; right panel; n = 9–10 each group). P210 immunization significantly reduced macrophage infiltration (B) assessed by MOMA-2 stain (n = 9–10 each group) and DC presence (C) assessed by CD11c (n = 7–12 each group) stain in aortic sinus plaques. Positive stain indicated by reddish-brown color. Data were analyzed by ANOVA followed by Newman-Keuls multiple group comparison, *P<0.05 vs. PBS and cBSA/alum.

From: Chyu K-Y, Zhao X, Dimayuga PC, Zhou J, Li X, Yano J, et al. (2012) CD8+ T Cells Mediate the Athero-Protective Effect of Immunization with an ApoB-100 Peptide.
PLoS ONE 7(2): e30780.

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Rat anti Mouse Macrophages/Monocytes antibody, clone MOMA-2 used for the detection of macrophages in aortic atherosclerotic lesions by immunohistochemistry on formalin fixed cryosections.
Image caption:
PBA treatment influenced the stability of plaque. Representative photomicrographs and the quantitative analysis of smooth muscle cell (SMC), CD3, macrophage (Mφ), and TUNEL in lesion of aortic root of ApoE-/- mice. The aortic root sections were stained with rabbit polyclonal to α- smooth muscle actin, rat anti-mouse macrophage Moma-2 and rat anti mouse CD3. The content of macrophage, smooth muscle cell, CD3 T cell in lesion was analyzed respectively by immunohistochemistry. For detection of cell apoptosis, sections were incubated with anti-TUNEL antibody and the content of apoptotic cells was analyzed by immunofluorescence. (n = 10 per group), *p<0.05, **p<0.01, ***p<0.001.

From: Wang B, Dai S, Dong Z, Sun Y, Song X, Guo C, et al. (2014) The Modulation of Endoplasmic Reticulum Stress by Chemical Chaperone Upregulates Immune Negative Cytokine IL-35 in Apolipoprotein E-Deficient Mice.
PLoS ONE 9(1): e87787.

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Rat anti Mouse Macrophages/Monocytes antibody, clone MOMA-2 used to evaluate macrophage influx to carotid artery atherosclerotic lesions by immunohistochemistry on formalin fixed cryosections.
Image caption:
Carotid plaque compositions in three groups of mice. A, Representative Sirius-red staining of collagen, Oil-red O staining of lipids, MOMA-2 immunostaining of macrophages and α-SMC-actin immunostaining in three groups of mice; (B) Quantification of staining results in three groups of mice. * P<0.05, ** P<0.01, ***P<0.001 vs. Ad-EGFP group.

From: Liu XL, Zhang PF, Ding SF, Wang Y, Zhang M, Zhao YX, et al. (2012) Local Gene Silencing of Monocyte Chemoattractant Protein-1 Prevents Vulnerable Plaque Disruption in Apolipoprotein E-Knockout Mice.
PLoS ONE 7(3): e33497.

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Rat anti Mouse Macrophages/Monocytes antibody, clone MOMA-2 used for the detection of macrophages in atherosclerotic plaques for the aortic sinus by immunohistochemistry on cryosections.
Image caption:
Effects of diet change on atherosclerotic plaques in aortic sinus from apoE-/- mice. (A) Representative photograph of Oil-Red-O and macrophage (MOMA-2) staining of atherosclerotic plaques in the aortic sinus of atherogenic diet (AD) and normal diet (ND) mice. Bar = 0.1 mm. (B) Representative photograph of CD3+ T cell staining of atherosclerotic plaques in the aortic sinus of atherogenic diet (AD) and normal diet (ND) mice. Bar = 0.1 mm. (C) Histomorphometric measurements of each staining are shown in bar graphs. N = 10 in each group for plaque size, lipid content and macrophage content. N = 5 in each group for CD3+ T cell content.

From: Chyu K-Y, Lio WM, Dimayuga PC, Zhou J, Zhao X, Yano J, et al. (2014) Cholesterol Lowering Modulates T Cell Function In Vivo and In Vitro. PLoS ONE 9(3): e92095.

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Rat anti Mouse Macrophages/Monocytes antibody, clone MOMA-2 used for the detection of macrophages in atherosclerotic plaques by immunohistochemistry on cryosections.
Image caption:
Lesion complexity does not differ with CCL3 bone marrow genotype. LDLR-/- mice were transplanted with C57BL/6 or CCL3-/- bone marrow. At four weeks post-BMT, mice were placed on WD for 12 weeks. ORO (4×), Trichrome, MOMA-2, and CD4 stained lesion (10×) are in columns as indicated on figure. Gender and donor marrow are indicated on the left of the figure. Sections were chosen from images representing mice with lesion areas close to the mean of their respective groups.

From: Kennedy A, Gruen ML, Gutierrez DA, Surmi BK, Orr JS, Webb CD, et al. (2012) Impact of Macrophage Inflammatory Protein-1α Deficiency on Atherosclerotic Lesion Formation, Hepatic Steatosis, and Adipose Tissue Expansion.
PLoS ONE 7(2): e31508.

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Rat anti Mouse Macrophages/Monocytes antibody, clone MOMA-2 used for the detection of macrophages in aortic sinus lesions using immunohistochemistry on formalin fixed cryosections.
Image caption:
The quantification of lesion area for macrophage abundance as calculated using Moma-positive staining.

From: Wang L, Yang M, Arias A, Song L, Li F, Tian F, et al. (2015) Splenocytes Seed Bone Marrow of Myeloablated Mice: Implication for Atherosclerosis.
PLoS ONE 10(6): e0125961.

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AlexaFluor®488 conjugated Rat anti Mouse macrophages and monocyte antibody, clone MOMA-2 used for the evaluation of macrophage antigen expression in vitro by immunofluorescence.
Image caption:
Inhibition of HDAC activity alters the phenotype of macrophages generated after 11 days of culture. (A-H) Immunocitochemistry of activated-macrophage markers, F4/80 and Moma-2. Pancake-like shape macrophages generated in the GM-CSF group are immunopositive for F4/80 (A and C) and Moma-2 (E and G). In the atypical elongated macrophages generated in the TSA + GM-CSF, the F4/80 and Moma-2 are down regulated (B, D, F and H—arrow). (I-P) Immunocitochemistry of M1 macrophage marker iNOS, and M2 macrophage marker, arginase 1. In the GM-CSF group, macrophages with pancake-like shape are immunopositive for iNOS (I and K) and for arginase 1 (M and O). The atypical elongated macrophage generated in the TSA + GM-CSF group are immunopositive for iNOS (J and L—arrow) and for arginase 1 (N and P—asterisk). Arginase 1 correlates to round cells in the GM-CSF group (M and O, asterisk) while in the TSA + GM-CSF group, the arginase 1 is associated only to elongated macrophages (N and P—asterisk).

From: Cabanel M, Brand C, Oliveira-Nunes MC, Cabral-Piccin MP, Lopes MF, Brito JM, et al. (2015) Epigenetic Control of Macrophage Shape Transition towards an Atypical Elongated Phenotype by Histone Deacetylase Activity. PLoS ONE 10(7): e0132984.

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Rat anti Mouse macrophages and monocytes antibody, clone MOMA-2 used for the demonstration of infiltrating macrophages in mouse retina by immunohistochemistry on cryosections.
Image caption:
Monocyte/Macrophage infiltration in sections from C57BL/6 and S100B KO mice. A, C57BL/6 WT retinal section from mouse with EAU showing cells staining positively for MOMA-2 (red). B, positive MOMA-2 staining in S100B KO with EAU was also observed in the rod outer segments and vitreous. No positively stained cells were observed in negative control staining in C57BL/6 mice (C) or S100B KO mice with EAU (D), where primary antibody was replaced with TBS. No positive staining was observed in naïve C57BL/6 WT (E) or S100B KO mice (F). Cells positive for MOMA-2 were counted in a total area of 1.5 mm2. An average cell number was calculated from 3 sections taken at spaced intervals through the eye. A significant reduction in positively stained cells was observed in S100B KO mice compared to C57BL/6 WT mice both in the retinal layers overall (G) and specifically within the rod outer segments (ROS) (H). Error bars indicate SEM; n = 8 randomly selected eyes per genotype. Scale bars indicate 100 μm.

From: Niven J, Hoare J, McGowan D, Devarajan G, Itohara S, Gannagé M, et al. (2015) S100B Up-Regulates Macrophage Production of IL1ß and CCL22 and Influences Severity of Retinal Inflammation.
PLoS ONE 10(7): e0132688.

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Rat anti Mouse Macrophages/Monocytes antibody, clone MOMA-2 used for the detection of mouse macrophages in atherosclerotic lesions by immunohistochemistry on cryosections.
Image caption:
Atherosclerotic lesions in aortic sinus. (A,B) Representative images of oil red O-stained atherosclerotic lesions in aortic sinus. (C,D) Immunohistochemical staining of macrophages (brown) in the cross-sections adjacent to the oil red O-stained images. (E) Quantitative analysis of the lesion area. Each dot indicates mean size of the oil red O-stained lesion area in each mouse. Bars indicate mean ± SEM of 8 mice for each group.

From: Shuto Y, Asai A, Nagao M, Sugihara H, Oikawa S (2015) Repetitive Glucose Spikes Accelerate Atherosclerotic Lesion Formation in C57BL/6 Mice.
PLoS ONE 10(8): e0136840.

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Rat anti Mouse Macrophages/Monocytes antibody, clone MOMA-2 used for the identification of infiltrating macrophages in atherosclerotic lesions by immunohistochemistry on formalin fixed cryosections.
Image caption:
SSAO inactivation stabilized the established atherosclerotic lesions under hypercholesterolemia.
Female LDLr KO mice were fed WTD for 6 weeks to induce the formation of atherosclerotic lesions. Thereafter, 0.125% semicarbazide were added in drinking water to inactivate SSAO during the subsequent 3 weeks (A) before the analysis of SSAO activities in the visceral adipose tissue (B), plasma cholesterol levels (C) and atherosclerotic lesions at the aortic root (D-G). (D) A scattered dot plot (left) or representative photomicrographs showing the size of atherosclerotic lesions. Sections were stained with oil-red-O (original magnification 40x, right panel). Each dot represents the mean lesion area of a single mouse, and the horizontal bar indicates the mean value of the group (left panel). (E) Representative photomicrographs showing macrophages and collagens in lesions. Sections of aortic roots were stained with antibodies against Moma-2 to visualize macrophages (brown, 100x) or with Masson’s Trichrome Accustain to visualize collagens (blue, 100x). (F & G) Bar graphs showing the lesion contents of macrophages (F), collagens (G), necrotic core (H) and cap thickness (I). Results were expressed as mean±SEM. Statistically significant difference *p<0.05, **p<0.01, and ***p<0.001 vs vehicle.

From: Peng Y, Wang J, Zhang M, Niu P, Yang M, Yang Y, et al. (2016)
Inactivation of Semicarbazide-Sensitive Amine Oxidase Stabilizes the Established Atherosclerotic Lesions via Inducing the Phenotypic Switch of Smooth Muscle Cells.
PLoS ONE 11(4): e0152758.

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Rat anti Mouse Macrophages/Monocytes antibody, clone MOMA-2 used for the identification of infiltrating macrophages in atherosclerotic lesions by immunohistochemistry on formalin fixed cryosections.
Image caption:
SSAO inactivation stabilized the established atherosclerotic lesions after normalization of hypercholesterolemia by diet lipid lowering.
Male LDLr KO mice were fed WTD for 9 weeks to induce the formation of atherosclerotic lesions. Thereafter, these animals were fed regular chow diet to normalize hypercholesterolemia (A). Drinking water containing 0.125% semicarbazide was given to these chow-fed animals in the subsequent 6 weeks (A) before the analysis of SSAO activities in the visceral adipose tissue (B), plasma cholesterol levels (C) or atherosclerotic lesions at the aortic root (D-G). (D) A scattered dot plot (left) or representative photomicrographs showing the size of atherosclerotic lesions. Sections were stained with oil-red-O (original magnification 40x, right panel). Each dot represents the mean lesion area of a single mouse, and the horizontal bar indicates the mean value of the group (left panel). (E) Representative photomicrographs showing the lesion contents of Moma-2+ macrophages (upper panel) or collagens (lower panel) in each group. Sections of aortic roots were stained with antibodies against Moma-2 to visualize macrophages (brown, 100x) or with Masson’s Trichrome Accustain to visualize collagens (blue, 100x). (F & G) Bar graphs showing the lesion contents of macrophages (F), collagens (G), necrotic core (H), and cap thickness (I) in vehicle- or semicarbazide-treated mice. Results were expressed as mean ±SEM. Statistically significant difference ***p<0.001 and *p<0.05 vs vehicle.

From: Peng Y, Wang J, Zhang M, Niu P, Yang M, Yang Y, et al. (2016)
Inactivation of Semicarbazide-Sensitive Amine Oxidase Stabilizes the Established Atherosclerotic Lesions via Inducing the Phenotypic Switch of Smooth Muscle Cells.
PLoS ONE 11(4): e0152758.

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Rat anti Mouse monocytes/macrophages antibody, clone MOMA-2 (MCA519G) used for the identification of infiltrating macrophages in a mouse model of Buruli ulcer by immunohistochemistry in formalin fixed paraffin embedded tisue sections along with Rat anti Mouse CD45R, clone RA3-6B2 (MCA1258G) to identify B cells and Rat anti Human CD3 antibody, clone CD3-12 (MCA1477) to identify T-cells. Neutrophils are stained using an anti neutrophil monoclonal antibody.
Image caption:
Infiltration of leukocytes within the footpad infected with M. ulcerans.
Immunohistochemistry was performed on 5 micrometer paraffin embedded sections of footpad of mice infected with a suspension of M. ulcerans (NM20/02) in order to identify the nature of the leukocytic infiltrate present within and around the bacterial foci. B cells were stained with anti-CD45R antibody (A), T cells with anti-CD3 antibody (B), Macrophages with MOMA (C) and neutrophils with anti-Ly6G/Ly6C (D).

From: Bénard A, Sala C, Pluschke G (2016)
Mycobacterium ulcerans Mouse Model Refinement for Pre-Clinical Profiling of Vaccine Candidates.
PLoS ONE 11(11): e0167059.

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  • Rat anti Mouse Macrophages/Monocytes:Alexa Fluor® 488
  • Rat anti Mouse Macrophages/Monocytes:RPE
  • Rat anti Mouse Macrophages/Monocytes:FITC
  • Rat anti Mouse Macrophages/Monocytes:FITC
  • Rat anti Mouse Macrophages/Monocytes
  • Rat anti Mouse Macrophages/Monocytes:Alexa Fluor® 647
  • Rat anti Mouse Macrophages/Monocytes:Alexa Fluor® 700
  • Rat anti Mouse Macrophages/Monocytes:Alexa Fluor® 647
  • Rat anti Mouse Macrophages/Monocytes:Alexa Fluor® 488
  • Rat anti Mouse Macrophages/Monocytes
  • Rat anti Mouse Macrophages/Monocytes:FITC
  • Rat anti Mouse Macrophages/Monocytes:RPE
  • Rat anti Mouse Macrophages/Monocytes:Alexa Fluor® 700
(Rated 0.0 out of 5 based on 0 customer reviews)
  • Product Type
    Monoclonal Antibody
  • Clone
    MOMA-2
  • Isotype
    IgG2b
6 Formats Available
    Product CodeApplicationsDatasheetMSDSPack SizeList PriceQuantity
    MCA519FFdatasheet pdfdatasheet pdf0.1 mg
    MCA519F
    MCA519GC, F *, IFdatasheet pdfdatasheet pdf0.25 mg
    MCA519G
    MCA519PEF *datasheet pdfdatasheet pdf100 Tests
    MCA519PE
    MCA519A647F *datasheet pdfdatasheet pdf100 Tests/1ml
    MCA519A647
    MCA519A488F *datasheet pdfdatasheet pdf100 Tests/1ml
    MCA519A488
    MCA519A700F *datasheet pdfdatasheet pdf100 Tests/1ml
    MCA519A700
    MCA519FTFdatasheet pdfdatasheet pdf25 µg
    MCA519FT
    MCA519GTC, F *, IFdatasheet pdfdatasheet pdf25 µg
    MCA519GT
    MCA519PETF *datasheet pdfdatasheet pdf25 Tests
    MCA519PET
    MCA519A488TF *datasheet pdfdatasheet pdf25 Tests/0.25ml
    MCA519A488T
    MCA519A647TF *datasheet pdfdatasheet pdf25 Tests/0.25ml
    MCA519A647T
    MCA519A700TF *datasheet pdfdatasheet pdf25 Tests/0.25ml
    MCA519A700T
    MCA519FAF *datasheet pdfdatasheet pdf50 µg
    MCA519FA
    Summary
    Secondary Antibodies
    Negative Isotype Controls
    Useful Reagents
    Positive Controls
    Histology Controls
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    References
    Reviews
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    • Rat anti Mouse Macrophages/Monocytes antibody, clone MOMA-2 recognizes an intracellular antigen of mouse macrophages and monocytes. It reacts strongly with macrophages in lymphoid organs such as tingible body macrophages and macrophages in T cell dependant areas and is extremely useful in immunohistochemistry. Reacts on all mouse strains tested.
    • Intended Use
    • Target Species
      Mouse
    • Product Form
      Purified IgG conjugated to Alexa Fluor®488 - liquid
      Purified IgG conjugated to R. Phycoerythrin (RPE) - lyophilised
      Purified IgG conjugated to Fluorescein Isothiocyanate Isomer 1 (FITC) - liquid
      Purified IgG conjugated to Fluorescein Isothiocyanate Isomer 1 (FITC) - liquid
      Purified IgG - liquid
      Purified IgG conjugated to Alexa Fluor®647 - liquid
      Purified IgG conjugated to Alexa Fluor®700 - liquid
      Purified IgG conjugated to Alexa Fluor®647 - liquid
      Purified IgG conjugated to Alexa Fluor®488 - liquid
      Purified IgG - liquid
      Purified IgG conjugated to Fluorescein Isothiocyanate Isomer 1 (FITC) - liquid
      Purified IgG conjugated to R. Phycoerythrin (RPE) - lyophilised
      Purified IgG conjugated to Alexa Fluor®700 - liquid
    • Reconstitution
      Pack Size: 100 TestsReconstitute with 1 ml distilled water
      Pack Size: 25 TestsReconstitute with 0.25 ml distilled water
      Pack Size: 100 TestsReconstitute with 1 ml distilled water
      Pack Size: 25 TestsReconstitute with 0.25 ml distilled water
    • Preparation
      Purified IgG prepared by affinity chromatography on Protein G from tissue culture supernatant
      Purified IgG prepared by affinity chromatography on Protein G from tissue culture supernatant
      Purified IgG prepared by affinity chromatography on Protein G from tissue culture supernatant
      Purified IgG prepared by affinity chromatography on Protein G from tissue culture supernatant
      Purified IgG prepared by affinity chromatography on Protein G from tissue culture supernatant
      Purified IgG prepared by affinity chromatography on Protein G from tissue culture supernatant
      Purified IgG prepared by affinity chromatography on Protein G from tissue culture supernatant
      Purified IgG prepared by affinity chromatography on Protein G from tissue culture supernatant
      Purified IgG prepared by affinity chromatography on Protein G from tissue culture supernatant
      Purified IgG prepared by affinity chromatography on Protein G from tissue culture supernatant
      Purified IgG prepared by affinity chromatography on Protein G from tissue culture supernatant
      Purified IgG prepared by affinity chromatography on Protein G from tissue culture supernatant
      Purified IgG prepared by affinity chromatography on Protein G from tissue culture supernatant
    • Preservative Stabilisers
      0.09%Sodium Azide
      1%Bovine Serum Albumin
      0.09%Sodium Azide
      1%Bovine Serum Albumin
      0.09%Sodium Azide
      1%Bovine Serum Albumin
      0.09%Sodium Azide
      1%Bovine Serum Albumin
      0.09%Sodium Azide
      0.09%Sodium Azide
      1%Bovine Serum Albumin
      0.09%Sodium Azide
      1%Bovine Serum Albumin
      0.09%Sodium Azide
      1%Bovine Serum Albumin
      0.09%Sodium Azide
      1%Bovine Serum Albumin
      0.09%Sodium Azide
      0.09%Sodium Azide
      1%Bovine Serum Albumin
      0.09%Sodium Azide
      1%Bovine Serum Albumin
      0.09%Sodium Azide
      1%Bovine Serum Albumin
    • Immunogen
      Mouse lymph node stroma.
    • Purity
    • Approx. Protein Concentrations
      IgG concentration 0.05mg/ml
      IgG concentration 0.1 mg/ml
      IgG concentration 0.1 mg/ml
      IgG concentration 0.5 mg/ml
      IgG concentration 0.05mg/ml
      IgG concentration 0.05mg/ml
      IgG concentration 0.05mg/ml
      IgG concentration 0.05mg/ml
      IgG concentration 0.5 mg/ml
      IgG concentration 0.1 mg/ml
      IgG concentration 0.05mg/ml
    • Reagents In The Kit
    • Preparing The Antibody
    • Test Principle
    • Buffer Solution
      Phosphate buffered saline
      Phosphate buffered saline
      Phosphate buffered saline
      Phosphate buffered saline
      Phosphate buffered saline
      Phosphate buffered saline
      Phosphate buffered saline
      Phosphate buffered saline
      Phosphate buffered saline
      Phosphate buffered saline
      Phosphate buffered saline
      Phosphate buffered saline
      Phosphate buffered saline
    • Fusion Partners
      Spleen cells from immunised Wistar rats were fused with cells of the SP/0 myeloma cell line.
    • Storage
      Store at +4oC or at -20oC if preferred.

      This product should be stored undiluted.

      Storage in frost free freezers is not recommended. This product is photosensitive and should be protected from light.

      Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.
      Prior to reconstitution store at +4oC.
      Following reconstitution store at +4oC.
      DO NOT FREEZE.

      This product should be stored undiluted. This product is photosensitive and should be protected from light. Should this product contain a precipitate we recommend microcentrifugation before use.
      Store at +4oC or at -20oC if preferred.

      This product should be stored undiluted.

      Storage in frost free freezers is not recommended. This product is photosensitive and should be protected from light.

      Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.
      Store at +4oC or at -20oC if preferred.

      This product should be stored undiluted.

      Storage in frost free freezers is not recommended. This product is photosensitive and should be protected from light.

      Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.
      Store at +4oC or at -20oC if preferred.

      This product should be stored undiluted.

      Storage in frost-free freezers is not recommended. Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.
      Store at +4oC or at -20oC if preferred.

      This product should be stored undiluted.

      Storage in frost free freezers is not recommended. This product is photosensitive and should be protected from light.

      Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.
      Store at +4oC or at -20oC if preferred.

      This product should be stored undiluted.

      Storage in frost free freezers is not recommended. This product is photosensitive and should be protected from light.

      Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.
      Store at +4oC or at -20oC if preferred.

      This product should be stored undiluted.

      Storage in frost free freezers is not recommended. This product is photosensitive and should be protected from light.

      Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.
      Store at +4oC or at -20oC if preferred.

      This product should be stored undiluted.

      Storage in frost free freezers is not recommended. This product is photosensitive and should be protected from light.

      Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.
      Store at +4oC or at -20oC if preferred.

      This product should be stored undiluted.

      Storage in frost-free freezers is not recommended. Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.
      Store at +4oC or at -20oC if preferred.

      This product should be stored undiluted.

      Storage in frost free freezers is not recommended. This product is photosensitive and should be protected from light.

      Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.
      Prior to reconstitution store at +4oC.
      Following reconstitution store at +4oC.
      DO NOT FREEZE.

      This product should be stored undiluted. This product is photosensitive and should be protected from light. Should this product contain a precipitate we recommend microcentrifugation before use.
      Store at +4oC or at -20oC if preferred.

      This product should be stored undiluted.

      Storage in frost free freezers is not recommended. This product is photosensitive and should be protected from light.

      Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.
    • Shelf Life
      18 months from date of despatch.
      12 months from date of reconstitution.
      18 months from date of despatch.
      18 months from date of despatch.
      18 months from date of despatch.
      18 months from date of despatch.
      18 months from date of despatch.
      18 months from date of despatch.
      18 months from date of despatch.
      18 months from date of despatch.
      18 months from date of despatch.
      12 months from date of reconstitution.
      18 months from date of despatch.
    • Acknowledgements
      This product is provided under an intellectual property licence from Life Technologies Corporation. The transfer of this product is contingent on the buyer using the purchase product solely in research, excluding contract research or any fee for service research, and the buyer must not sell or otherwise transfer this product or its components for (a) diagnostic, therapeutic or prophylactic purposes; (b) testing, analysis or screening services, or information in return for compensation on a per-test basis; (c) manufacturing or quality assurance or quality control, or (d) resale, whether or not resold for use in research. For information on purchasing a license to this product for purposes other than as described above, contact Life Technologies Corporation, 5791 Van Allen Way, Carlsbad CA 92008 USA or outlicensing@thermofisher.com
      This product is provided under an intellectual property licence from Life Technologies Corporation. The transfer of this product is contingent on the buyer using the purchase product solely in research, excluding contract research or any fee for service research, and the buyer must not sell or otherwise transfer this product or its components for (a) diagnostic, therapeutic or prophylactic purposes; (b) testing, analysis or screening services, or information in return for compensation on a per-test basis; (c) manufacturing or quality assurance or quality control, or (d) resale, whether or not resold for use in research. For information on purchasing a license to this product for purposes other than as described above, contact Life Technologies Corporation, 5791 Van Allen Way, Carlsbad CA 92008 USA or outlicensing@thermofisher.com
      The Alexa Fluor® dye antibody conjugates in this product are sold under license from Molecular Probes, Inc. for research use only, except for use in combination with microarrays, and are covered by pending and issued patents.
      This product is provided under an intellectual property licence from Life Technologies Corporation. The transfer of this product is contingent on the buyer using the purchase product solely in research, excluding contract research or any fee for service research, and the buyer must not sell or otherwise transfer this product or its components for (a) diagnostic, therapeutic or prophylactic purposes; (b) testing, analysis or screening services, or information in return for compensation on a per-test basis; (c) manufacturing or quality assurance or quality control, or (d) resale, whether or not resold for use in research. For information on purchasing a license to this product for purposes other than as described above, contact Life Technologies Corporation, 5791 Van Allen Way, Carlsbad CA 92008 USA or outlicensing@thermofisher.com
      This product is provided under an intellectual property licence from Life Technologies Corporation. The transfer of this product is contingent on the buyer using the purchase product solely in research, excluding contract research or any fee for service research, and the buyer must not sell or otherwise transfer this product or its components for (a) diagnostic, therapeutic or prophylactic purposes; (b) testing, analysis or screening services, or information in return for compensation on a per-test basis; (c) manufacturing or quality assurance or quality control, or (d) resale, whether or not resold for use in research. For information on purchasing a license to this product for purposes other than as described above, contact Life Technologies Corporation, 5791 Van Allen Way, Carlsbad CA 92008 USA or outlicensing@thermofisher.com
      This product is provided under an intellectual property licence from Life Technologies Corporation. The transfer of this product is contingent on the buyer using the purchase product solely in research, excluding contract research or any fee for service research, and the buyer must not sell or otherwise transfer this product or its components for (a) diagnostic, therapeutic or prophylactic purposes; (b) testing, analysis or screening services, or information in return for compensation on a per-test basis; (c) manufacturing or quality assurance or quality control, or (d) resale, whether or not resold for use in research. For information on purchasing a license to this product for purposes other than as described above, contact Life Technologies Corporation, 5791 Van Allen Way, Carlsbad CA 92008 USA or outlicensing@thermofisher.com
    • Regulatory
      For research purposes only
    • This product has been reported to work in the following applications. This information is derived from testing within our laboratories, peer-reviewed publications or personal communications from the originators. Please refer to references indicated for further information. For general protocol recommendations, please visit the antibody protocols page.

    • Application NameYesNoMin DilutionMax Dilution
      Flow Cytometry(1)Neat1/10
      (1)
      Membrane permeabilisation is required for this application. Bio-Rad recommends the use of Leucoperm™ (Product Code BUF09) for this purpose.
    • Application NameYesNoMin DilutionMax Dilution
      Flow Cytometry(1)Neat1/10
      (1)
      Membrane permeabilisation is required for this application. Bio-Rad recommends the use of Leucoperm™ (Product Code BUF09) for this purpose.
    • Application NameYesNoMin DilutionMax Dilution
      Flow Cytometry(1)Neat1/10
      (1)
      Membrane permeabilisation is required for this application. Bio-Rad recommends the use of Leucoperm™ (Product Code BUF09) for this purpose.
    • Application NameYesNoMin DilutionMax Dilution
      Flow Cytometry(1)Neat1/10
      (1)
      Membrane permeabilisation is required for this application. Bio-Rad recommends the use of Leucoperm™ (Product Code BUF09) for this purpose.
    • Application NameYesNoMin DilutionMax Dilution
      Immunofluorescence
      Immunohistology - Frozen1/25
      Flow Cytometry(1)
      (1)
      Membrane permeabilisation is required for this application. Bio-Rad recommends the use of Leucoperm™ (Product Code BUF09) for this purpose.
    • Application NameYesNoMin DilutionMax Dilution
      Flow Cytometry(1)Neat1/10
      (1)
      Membrane permeabilisation is required for this application. Bio-Rad recommends the use of Leucoperm™ (Product Code BUF09) for this purpose.
    • Application NameYesNoMin DilutionMax Dilution
      Flow Cytometry(1)Neat1/10
      (1)
      Membrane permeabilisation is required for this application. Bio-Rad recommends the use of Leucoperm™ (Product Code BUF09) for this purpose.
    • Application NameYesNoMin DilutionMax Dilution
      Flow Cytometry(1)Neat1/10
      (1)
      Membrane permeabilisation is required for this application. Bio-Rad recommends the use of Leucoperm™ (Product Code BUF09) for this purpose.
    • Application NameYesNoMin DilutionMax Dilution
      Flow Cytometry(1)Neat1/10
      (1)
      Membrane permeabilisation is required for this application. Bio-Rad recommends the use of Leucoperm™ (Product Code BUF09) for this purpose.
    • Application NameYesNoMin DilutionMax Dilution
      Immunofluorescence
      Immunohistology - Frozen1/25
      Flow Cytometry(1)
      (1)
      Membrane permeabilisation is required for this application. Bio-Rad recommends the use of Leucoperm™ (Product Code BUF09) for this purpose.
    • Application NameYesNoMin DilutionMax Dilution
      Flow Cytometry(1)Neat1/10
      (1)
      Membrane permeabilisation is required for this application. Bio-Rad recommends the use of Leucoperm™ (Product Code BUF09) for this purpose.
    • Application NameYesNoMin DilutionMax Dilution
      Flow Cytometry(1)Neat1/10
      (1)
      Membrane permeabilisation is required for this application. Bio-Rad recommends the use of Leucoperm™ (Product Code BUF09) for this purpose.
    • Application NameYesNoMin DilutionMax Dilution
      Flow Cytometry(1)Neat1/10
      (1)
      Membrane permeabilisation is required for this application. Bio-Rad recommends the use of Leucoperm™ (Product Code BUF09) for this purpose.

    • Where this antibody has not been tested for use in a particular technique this does not necessarily exclude its use in such procedures. Suggested working dilutions are given as a guide only. It is recommended that the user titrates the antibody for use in their own system using appropriate negative/positive controls.

      *Membrane permeabilisation is required for this application. Bio-Rad recommends the use of Leucoperm (Product Code BUF09) for this purpose.
    • Technical Advice
    • Technical Advice
    • Technical Advice
    • Technical Advice
    • Technical Advice
    • Technical Advice
    • Technical Advice
    • Technical Advice
    • Technical Advice
    • Technical Advice
    • Technical Advice
    • Technical Advice
    • Technical Advice
    • Recommended Protocol
    • Recommended Protocol
    • Recommended Protocol
    • Recommended Protocol
    • Recommended Protocol
    • Recommended Protocol
    • Recommended Protocol
    • Recommended Protocol
    • Recommended Protocol
    • Recommended Protocol
    • Recommended Protocol
    • Recommended Protocol
    • Recommended Protocol
    • ELISA
    • ELISA
    • ELISA
    • ELISA
    • ELISA
    • ELISA
    • ELISA
    • ELISA
    • ELISA
    • ELISA
    • ELISA
    • ELISA
    • ELISA
    • Immunohistology
    • Immunohistology
    • Immunohistology
    • Immunohistology
    • Immunohistology
    • Immunohistology
    • Immunohistology
    • Immunohistology
    • Immunohistology
    • Immunohistology
    • Immunohistology
    • Immunohistology
    • Immunohistology
    • Histology Positive Control Tissue
    • Histology Positive Control Tissue
    • Histology Positive Control Tissue
    • Histology Positive Control Tissue
    • Histology Positive Control Tissue
    • Histology Positive Control Tissue
    • Histology Positive Control Tissue
    • Histology Positive Control Tissue
    • Histology Positive Control Tissue
    • Histology Positive Control Tissue
    • Histology Positive Control Tissue
    • Histology Positive Control Tissue
    • Histology Positive Control Tissue
    • Immunofluorescence
    • Immunofluorescence
    • Immunofluorescence
    • Immunofluorescence
    • Immunofluorescence
    • Immunofluorescence
    • Immunofluorescence
    • Immunofluorescence
    • Immunofluorescence
    • Immunofluorescence
    • Immunofluorescence
    • Immunofluorescence
    • Immunofluorescence
    • Western Blotting
    • Western Blotting
    • Western Blotting
    • Western Blotting
    • Western Blotting
    • Western Blotting
    • Western Blotting
    • Western Blotting
    • Western Blotting
    • Western Blotting
    • Western Blotting
    • Western Blotting
    • Western Blotting
    • Instructions For Use
    • Instructions For Use
    • Instructions For Use
    • Instructions For Use
    • Instructions For Use
    • Instructions For Use
    • Instructions For Use
    • Instructions For Use
    • Instructions For Use
    • Instructions For Use
    • Instructions For Use
    • Instructions For Use
    • Instructions For Use

    Additional Macrophages/Monocytes Antibody Formats

    Formats Clone Applications Sizes available
    Macrophages/Monocytes Antibody : Alexa Fluor® 647 MOMA-2 F * 100 Tests/1ml | 25 Tests/0.25ml
    Macrophages/Monocytes Antibody : Alexa Fluor® 488 MOMA-2 F * 25 Tests/0.25ml | 100 Tests/1ml
    Macrophages/Monocytes Antibody : Purified MOMA-2 C, F *, IF 0.25 mg | 25 µg
    Macrophages/Monocytes Antibody : FITC MOMA-2 F, F * 25 µg | 0.1 mg | 50 µg
    Macrophages/Monocytes Antibody : RPE MOMA-2 F * 100 Tests | 25 Tests
    Macrophages/Monocytes Antibody : Alexa Fluor® 700 MOMA-2 F * 25 Tests/0.25ml | 100 Tests/1ml
    • Copyright © 2016 Bio-Rad Antibodies (formerly AbD Serotec)

    Recommended Secondary Antibody

      DescriptionProduct CodePack SizeApplicationsList PriceQuantity
      Goat anti Rat IgG:Alk. Phos. (Mouse Adsorbed)STAR131A1 mlC, E, P, WB
      STAR131A
      Goat anti Rat IgG:Biotin (Mouse Adsorbed)STAR131B0.5 mgC, E, IF, P, WB
      STAR131B
      Goat anti Rat IgG:DyLight®549 (Mouse Adsorbed)STAR71D549GA0.1 mgF, IF
      STAR71D549GA
      Goat anti Rat IgG:DyLight®649 (Mouse Adsorbed)STAR71D649GA0.1 mgF, IF
      STAR71D649GA
      Rabbit F(ab')2 anti Rat IgG:Dylight®800STAR16D800GA0.1 mgF, IF, WB
      STAR16D800GA
      Goat anti Rat IgG:Dylight®800 (Mouse Adsorbed)STAR71D800GA0.1 mgF, IF, WB
      STAR71D800GA
      Goat F(ab')2 anti Rat IgG:FITC (Mouse Adsorbed)STAR690.5 mlF
      STAR69
      Rabbit F(ab')2 anti Rat IgG:FITCSTAR17B1 mgF
      STAR17B
      Goat anti Rat IgG:HRP (Mouse Adsorbed)STAR720.5 mgC, E, P
      STAR72
      Rabbit F(ab')2 anti Rat IgG:HRPSTAR21B1 mgC, E, P, RE
      STAR21B
      Goat F(ab')2 anti Rat IgG:RPE (Mouse Adsorbed)STAR730.5 mlF
      STAR73
      Rabbit F(ab')2 anti Rat IgG:RPESTAR20A1 mlF
      STAR20A
      DescriptionProduct CodePack SizeApplicationsList PriceQuantity
      Goat anti Rat IgG:Alk. Phos. (Mouse Adsorbed)STAR131A1 mlC, E, P, WB
      STAR131A
      Goat anti Rat IgG:Biotin (Mouse Adsorbed)STAR131B0.5 mgC, E, IF, P, WB
      STAR131B
      Goat anti Rat IgG:DyLight®549 (Mouse Adsorbed)STAR71D549GA0.1 mgF, IF
      STAR71D549GA
      Goat anti Rat IgG:DyLight®649 (Mouse Adsorbed)STAR71D649GA0.1 mgF, IF
      STAR71D649GA
      Rabbit F(ab')2 anti Rat IgG:Dylight®800STAR16D800GA0.1 mgF, IF, WB
      STAR16D800GA
      Goat anti Rat IgG:Dylight®800 (Mouse Adsorbed)STAR71D800GA0.1 mgF, IF, WB
      STAR71D800GA
      Goat F(ab')2 anti Rat IgG:FITC (Mouse Adsorbed)STAR690.5 mlF
      STAR69
      Rabbit F(ab')2 anti Rat IgG:FITCSTAR17B1 mgF
      STAR17B
      Goat anti Rat IgG:HRP (Mouse Adsorbed)STAR720.5 mgC, E, P
      STAR72
      Rabbit F(ab')2 anti Rat IgG:HRPSTAR21B1 mgC, E, P, RE
      STAR21B
      Goat F(ab')2 anti Rat IgG:RPE (Mouse Adsorbed)STAR730.5 mlF
      STAR73
      Rabbit F(ab')2 anti Rat IgG:RPESTAR20A1 mlF
      STAR20A

      Recommended Negative Isotype Control

        DescriptionProduct CodePack SizeApplicationsList PriceQuantity
        Rat IgG2b Negative Control:Alexa Fluor® 700MCA1125A700100 Tests/1mlF
        MCA1125A700
        DescriptionProduct CodePack SizeApplicationsList PriceQuantity
        Rat IgG2b Negative Control:Alexa Fluor® 700MCA1125A700100 Tests/1mlF
        MCA1125A700

        Useful Reagents

          DescriptionProduct CodePack SizeApplicationsList PriceQuantity
          Mouse Seroblock FcRBUF041A0.1 mgF
          BUF041A
          Mouse Seroblock FcRBUF041B0.5 mgF
          BUF041B
          DescriptionProduct CodePack SizeApplicationsList PriceQuantity
          Mouse Seroblock FcRBUF041A0.1 mgF
          BUF041A
          Mouse Seroblock FcRBUF041B0.5 mgF
          BUF041B
          DescriptionProduct CodePack SizeApplicationsList PriceQuantity
          Mouse Seroblock FcRBUF041A0.1 mgF
          BUF041A
          Mouse Seroblock FcRBUF041B0.5 mgF
          BUF041B
          DescriptionProduct CodePack SizeApplicationsList PriceQuantity
          Mouse Seroblock FcRBUF041A0.1 mgF
          BUF041A
          Mouse Seroblock FcRBUF041B0.5 mgF
          BUF041B
          DescriptionProduct CodePack SizeApplicationsList PriceQuantity
          Mouse Seroblock FcRBUF041A0.1 mgF
          BUF041A
          Mouse Seroblock FcRBUF041B0.5 mgF
          BUF041B

          Recommended Positive Controls

            Histology Controls

              Source Reference

              References

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