CD321 antibody | M.Ab.F11
Mouse anti Human CD321 antibody, clone F11 (MCA2270) used for the visualization of CD321 expression on microvascular endothelial cells in vitro by immunofluorescence.
Image caption:
Immunocytochemical JAM-A tight junction staining in primary HBMEC is reduced under barrier-disturbing pro-inflammatory conditions.
Cells were either left unstimulated or treated with TNF-α 10 ng/mL and IFN-γ 100 U/mL for 24 h.
Immunocytochemical staining was performed with primary antibodies against JAM-A (M.Ab.F11). Representative for 5 independent experiments with different HBMEC preparations. Bar = 25μm.
From: Haarmann A, Deiß A, Prochaska J, Foerch C, Weksler B, Romero I, et al. (2010)
Evaluation of Soluble Junctional Adhesion Molecule-A as a Biomarker of Human Brain Endothelial Barrier Breakdown.
PLoS ONE 5(10): e13568.
This image is from an open access article distributed under the terms of the Creative Commons Attribution License.
Mouse anti Human CD321 antibody, clone F11 (MCA2270) used for the evaluation of CD321 expression on microvascular endothelial cells in vitro by flow cytometry.
Image caption:
In contrast to ICAM-1, JAM-A overall surface expression levels on HBMEC do not change upon pro-inflammatory stimulation.
Flow cytometric analysis of Accutase™-dissociated single cell suspensions of primary HBMEC after stimulation as in Figure 1. JAM-A was stained with M.Ab.F11 and a rabbit polyclonal antibody from Zymed. Staining against ICAM-1 served as a positive control. In parallel, unstimulated and stimulated HBMEC were stained with matched isotype control antibodies. Filled histograms represent isotype stainings, open histograms JAM-A and ICAM-1 stainings. Representative for 5 independent experiments with different HBMEC preparations.
From: Haarmann A, Deiß A, Prochaska J, Foerch C, Weksler B, Romero I, et al. (2010)
Evaluation of Soluble Junctional Adhesion Molecule-A as a Biomarker of Human Brain Endothelial Barrier Breakdown.
PLoS ONE 5(10): e13568.
This image is from an open access article distributed under the terms of a Creative Commons Attribution License.
Mouse anti Human CD321 antibody, clone F11 (MCA2270) used for the evaluation of CD321 expression on microvascular endothelial cells in vitro by western blotting.
Image caption:
Pro-inflammatory stimulation of HBMEC induces JAM-A dissociation from the actin cytoskeleton.
A Primary HBMEC were either left unstimulated or treated with TNF-α 10 ng/mL or IFN-γ 100 IU/mL alone or in combination. Cell protein extracts were generated with a Nonidet-P40 based cell lysis buffer and subjected to Western blot analysis. JAM-A was stained with M.Ab.F11. Staining of the same, peroxidase-inactivated membranes with a rabbit antibody against β-actin served as a loading control. B N-deglycosylation of JAM-A with increasing concentrations of PNGase F for 2 h. A rabbit polyclonal antibody against JAM-A (Zymed) was used for the detection of JAM-A. The asterisk represents N-glycosylated, the open circle N-declycosylated JAM-A. Representative experiments out of at least 5 independent experiments with different EC preparations for each subpanel of the figure are shown.
From: Haarmann A, Deiß A, Prochaska J, Foerch C, Weksler B, Romero I, et al. (2010)
Evaluation of Soluble Junctional Adhesion Molecule-A as a Biomarker of Human Brain Endothelial Barrier Breakdown.
PLoS ONE 5(10): e13568.
This image is from an open access article distributed under the terms ofa Creative Commons Attribution License.
Mouse anti Human CD321 antibody, clone F11 recognizes human Junctional adhesion molecule A, also known as CD321, JAM-1, JAM-A, Platelet F11 receptor, Platelet adhesion molecule 1 or PAM-1. CD321 is a 272 amino acid ~35 kDa single pass type 1 transmembrane glycoprotein expressed by endothelium, epithelial tissues and some leukocytes (Ostermann et al. 2002). CD321 was originally identified as the F11 receptor expressed on platelets (Kornecki et al. 1990).
Mouse anti Human CD321 antibody, clone F11 is able to activate platelets, leading to aggregation and granule secretion (Kornecki et al. 1990, Naik et al. 1995).
Mouse anti Human CD321 antibody, clone F11 is able to activate platelets, leading to aggregation and granule secretion (Kornecki et al. 1990, Naik et al. 1995).
Product Details
- Target Species
- Human
- Product Form
- Purified IgG - liquid
- Buffer Solution
- Phosphate buffered saline
- Preservative Stabilisers
- <0.1% Sodium Azide (NaN3)
- Immunogen
- Human platelet membranes.
- Approx. Protein Concentrations
- IgG concentration 0.5 mg/ml
- Fusion Partners
- Spleen cells from immunized Balb/c mice were fused with cells of the mouse SP2/0 myeloma cell line.
Storage Information
- Storage
- This product is shipped at ambient temperature. It is recommended to aliquot and store at -20°C on receipt. When thawed, aliquot the sample as needed. Keep aliquots at 2-8°C for short term use (up to 4 weeks) and store the remaining aliquots at -20°C.
Avoid repeated freezing and thawing as this may denature the antibody. Storage in frost-free freezers is not recommended. - Guarantee
- 12 months from date of despatch
More Information
- UniProt
- Q9Y624
- Entrez Gene
- F11R
- GO Terms
- GO:0007596 blood coagulation
- GO:0016021 integral to membrane
- GO:0005923 tight junction
- GO:0006954 inflammatory response
- GO:0044419 interspecies interaction between organisms
- GO:0050900 leukocyte migration
- GO:0070830 tight junction assembly
- Regulatory
- For research purposes only
Applications of CD321 antibody
| Application Name | Verified | Min Dilution | Max Dilution |
|---|---|---|---|
| Flow Cytometry | 1/10 | 1/50 | |
| Functional Assays 1 | |||
| Immunofluorescence | |||
| Immunoprecipitation | |||
| Western Blotting | 1/100 | 1/1000 |
- 1 This product contains sodium azide, removal by dialysis is recommended prior to use in functional assays.
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.
- Flow Cytometry
- Use 10ul of the suggested working dilution to label 106 cells in 100ml
- Western Blotting
- MCA2270 detects a band of approximately 35-40kDa in platelet cell lysates.
Copyright © 2021 Bio-Rad Antibodies (formerly AbD Serotec)
Secondary Antibodies Available
Negative Isotype Controls Available
| Description | Product Code | Applications | Pack Size | List Price | Quantity |
|---|---|---|---|---|---|
| Mouse IgG1 Negative Control | MCA928 | F | 100 Tests |
|
Product Specific References
Source Reference
-
Kornecki, E. et al. (1990) Activation of human platelets by a stimulatory monoclonal antibody.
J Biol Chem. 265 (17): 10042-8.
References for CD321 antibody
-
Sobocka, M.B. et al. (2000) Cloning of the human platelet F11 receptor: a cell adhesion molecule member of the immunoglobulin superfamily involved in platelet aggregation.
Blood. 95 (8): 2600-9. -
Fraemohs, L. et al. (2004) The functional interaction of the beta 2 integrin lymphocyte function-associated antigen-1 with junctional adhesion molecule-A is mediated by the I domain.
J Immunol. 173 (10): 6259-64. -
Immenschuh, S. et al. (2009) Transcriptional induction of junctional adhesion molecule-C gene expression in activated T cells.
J Leukoc Biol. 85 (5): 796-803. -
Haarmann, A. et al. (2010) Evaluation of soluble junctional adhesion molecule-A as a biomarker of human brain endothelial barrier breakdown.
PLoS One. 5 (10): e13568.
Fluorescent Spectraviewer
Watch the Tool Tutorial Video ▸How to Use the Spectraviewer
Watch the Tool Tutorial Video ▸- Start by selecting the application you are interested in, with the option to select an instrument from the drop down menu or create a customized instrument
- Select the fluorophores or fluorescent proteins you want to include in your panel to check compatibility
- Select the lasers and filters you wish to include
- Select combined or multi-laser view to visualize the spectra
