Green Fluorescent Protein antibody
Sheep antiGreen Fluorescent protein antibody (4745-1051) used to detect GFP tagged constructs (CG8784:p65) in Drosophila larvae by immunofluorescence.
Image caption:
Hugin neurons target neurosecretory cells via peptide-receptor transmission in addition to synaptic connections. A, Promoter-based hugin receptor PK2-R1 driver line CG8784-Gal4::p65 was generated by replacing the first coding exon of the CG8784 loci with GAL4 in a BAC clone containing 80kb flanking genomic context and integrating the final BAC into attP site VK00033. B, CG8784-Gal4::p65 drives expression in cells of the pars intercerebralis (PI). C, Co-staining with Drosophila insulin-like peptide 2 (Dilp2), diuretic hormone 44 (DH44) and Dromyosuppressin (DMS). These peptides are produced by medial neurosecretory cells (mNSCs) in a non-overlapping manner. CG8784-Gal4::p65 drives expression in all mNSCs of the PI. Scale bars in A and B represent 10 &mum.
From: Schlegel P, Texada MJ, Miroschnikow A, Schoofs A, Hückesfeld S, Peters M,Schneider-Mizell CM, Lacin H, Li F, Fetter RD, Truman JW, Cardona A, Pankratz MJ.
Synaptic transmission parallels neuromodulation in a central food-intake circuit.
Elife. 2016 Nov 15;5. pii: e16799.
This image is from an open access article distributed under the terms of the Creative Commons Attribution License.
Sheep anti green fluorescent protein antibody (4745-1051) used for the detection of GFP tagged protein by immunofluorescence.
Image caption:
Khc is dispensable for early eye pattern formation. (A) A null mutant, khc8, was utilized to generate mutant clones in developing third-instar larval eye discs. Crb (apical marker, red) and E-cad (AJ maker, blue) showed little defects in third-instar larval eye discs. (B) A magnified view of (A). Mutant clones were marked by the absence of GFP (green).
From: League GP, Nam S-C (2011)
Role of Kinesin Heavy Chain in Crumbs Localization along the Rhabdomere Elongation in Drosophila Photoreceptor.
PLoS ONE 6(6): e21218.
This image is from an open access article distributed under the terms of a Creative Commons Attribution License.
Sheep anti green fluorescent protein antibody (4745-1051)used for the detection of GFP tagged protein by immunofluorescence.
Image caption:
Khc is essential for photoreceptor morphogenesis. khc8 mosaic clone in mid-stage (50% pd) pupal Drosophila photoreceptors. (A–E) khc8 Drosophila photoreceptors stained for Crb (apical marker, red), and E-cad (AJ marker, blue). (A′–E′) khc8 mutant photoreceptors were marked by the absence of GFP (green). As the cross sections move more proximally (A–E) both the apical Crb domain (red) and the AJs (blue) show increasingly severe defects. Crb (red) is misshapen at the distal section (A, B) and almost absent at the proximal section (E) from the same pupal eye. (F) Developing pupal photoreceptors elongate from distal to proximal direction. Distal (A, B) and proximal (D, E) sections are marked by dashed-lines.
From: League GP, Nam S-C (2011)
Role of Kinesin Heavy Chain in Crumbs Localization along the Rhabdomere Elongation in Drosophila Photoreceptor.
PLoS ONE 6(6): e21218.
This image is from an open access article distributed under the terms of a Creative Commons Attribution License.
Sheep anti green fluorescent protein antibody (4745-1051) used for the detection of GFP tagged protein by immunofluorescence.
Image caption:
Khc is essential for acetylated microtubules and AJ localization. Stabilized microtubules were stained with Acetub (red), AJs with E-cad (blue), and wild type cells with GFP (green). (A-A′) Distal regions of khc8 mutant photoreceptors, marked by the absence of GFP (green), display reduction and shrinkage of microtubules (arrow) compared to wild-type cells (double-arrow) and AJs (arrowhead) at the same location. (B-B′) Proximal regions of khc8 mutant photoreceptors display more severe defects of acetylated microtubules (arrow) and AJs (arrowhead).
From: League GP, Nam S-C (2011)
Role of Kinesin Heavy Chain in Crumbs Localization along the Rhabdomere Elongation in Drosophila Photoreceptor.
PLoS ONE 6(6): e21218.
This image is from an open access article distributed under the terms of a Creative Commons Attribution License.
Sheep anti green fluorescent protein antibody (4745-1051) used for the detection of GFP tagged protein by immunofluorescence.
Image caption:
Overexpression of Khc causes severe reduction of acetylated microtubules and apical domain. Khc-GFP overexpression causes severe reduction of the apical membrane domain in developing pupal eyes (45% pd). (A, B) Localization of Crb (apical marker, red) and E-cad (AJ marker, blue) in the sev-Gal4/+ control (A), and Khc-GFP overexpression by sev-Gal4 (B). Khc-GFP was marked by GFP (green, B′). Khc-GFP caused a loss of Crb (red, arrow, B) and mislocalization of E-cad (blue). (C, D) Localization of Acetub (stabilized microtubule marker, red) and Crb (apical marker, blue) in the sev-Gal4/+ control (C), and sev>Khc-GFP (D). Gal4 caused the reduction of Acetub (red, arrow, D) and Crb (blue). Khc-GFP was marked by GFP (green, D′).
From: League GP, Nam S-C (2011)
Role of Kinesin Heavy Chain in Crumbs Localization along the Rhabdomere Elongation in Drosophila Photoreceptor.
PLoS ONE 6(6): e21218.
This image is from an open access article distributed under the terms of a Creative Commons Attribution License.
Sheep anti green fluorescent protein antibody (4745-1051) used for the detection of GFP by immunofluorescence.
Image caption:
Properties of NG2 cell processes.
(A–D) Two-photon time-lapse recordings. (A) Overview of an Alexa-594-labeled NG2/EYFP cell (maximum projection, 100 μm x 100 μm x 15 μm, 60 equidistant planes, scale 10 μm). (B–D) Pairs of maximum projections (16 μm x 14 μm x 5 μm, 20 planes, scale 2 μm) taken at time points t0 (left) and t0 + Δt (right). Arrows mark processes that were elongated (B, Δt = 185 s) or retracted (C, Δt = 370 s). Additionally we observed varicosities traveling along the process (D, Δt = 370 s, start and end point marked by arrows). See also Videos S2, S3. (E–H) NG2 cell processes do not contain α-tubulin and PDI. Cortical tissue from an hGFAP/EGFP mouse (p13) was freshly dissociated and quadruple-stained with a nuclear marker (bisbenzimidine, blue) and antibodies against GFAP (also blue channel), GFP (green) and one of the proteins of interest (red): &apha;-tubulin (E), β-actin (F), ezrin (G) or the ER marker PDI (H). The cells analyzed were GFAP negative, GFP positive. Note nearby GFP negative cells (overviews, left in F–H, E). Areas boxed in the overviews (F–H) are enlarged for colocalization analysis. β-actin and ezrin were localized in the NG2 cell processes. Note the fine dimensions of these varicose processes visualized in the GFP channel (green). The PDI signal is present both in a non-identified, nearby cell (H, overview) and in the soma of the NG2 cell, but not in its processes (H, red, merge). The same is observed for α-tubulin (E red, merge). Note that α-tubulin/microtubules are well-preserved in the processes of nearby non-identified cells (E, merge) and of GFAP positive astrocytes (cf. Fig. S1). Scale bar 5 μm.
From: Haberlandt C, Derouiche A, Wyczynski A, Haseleu J, Pohle J, et al. (2011)
Gray Matter NG2 Cells Display Multiple Ca2+-Signaling Pathways and Highly Motile Processes.
PLoS ONE 6(3): e17575.
This image is from an open access article distributed under the terms of a Creative Commons Attribution License.
Sheep anti green fluorescent protein antibody (4745-1051) used for the detection of GFP tagged Hb9 neurons by immunofluorescence.
Image caption:
Gfrα1-TLZ+/Hb9::GFP- motor neurons display structural and synaptic characteristics of gamma motor neurons. (A) Neurolucida tracings of P20 large Gfrα1-TLZ-/Hb9::GFP+ (black) and small strongly Gfrα1-TLZ+/Hb9::GFP- MNs (gray). (B-D) Quantitative analyses of dendritic arbors. Gfr&apha;1-TLZ-/Hb9::GFP+ MN primary dendrites are more numerous, more highly branched (B) and thicker (C), than those of Gfrα1+/Hb9::GFP- MNs. Sholl analysis (D) of Gfrα1-TLZ-/Hb9::GFP+ (black line) and Gfrα1-TLZ+/Hb9::GFP- (gray line) MNs also reveals differences in the distribution of membrane surface at different distances from soma that are characteristic of α- vs. γ-MNs. (E) VGluT1+ contacts (red) are present on P20 Hb9::GFP+ (green) MNs, but absent on Gfrα1-TLZ+ (blue)/Hb9::GFP- neurons. (F) VAChT+ contacts (red) are present on both Hb9::GFP+ (green) and Gfrα1-TLZ+ (blue)/Hb9::GFP- MNs (E and F, regions in white boxes are magnified in insets). (G) Quantification of dendritic and somatic VGluT1 and VAChT positive contacts on Hb9::GFP+ (black bars) and Gfrα1-TLZ+/Hb9::GFP- (gray bars) MNs (error bars indicate SEMs; triple and double asterisks indicate significance levels of P<0.001 and P<0.01 in t-test comparisons, respectively). (H-K) Tibialis anterior muscle in a Hb9::GFP mouse showing Cy5-bungarotoxin (Cy5-Bgtx, blue) labeled intra- and extrafusal neuromuscular junctions (NMJ) and PGP9.5 immunolabeled sensory and motor axons (red). Hb9::GFP+ motor axons are in green (H). Spindle afferent annulospiral endings (dual asterisks; also shown in the inset in a serial section) and intrafusal muscle fibers are labeled with PGP9.5. Extrafusal NMJs are innervated by PGP9.5+ and Hb9::GFP+ motor axons (K, high magnification of boxed area). Most motor end-plates on intrafusal fibers lacked GFP. Intrafusal Cy5-Bgtx NMJs (white arrowheads) are innervated by PGP9.5-IR axons that are HB9::GFP- (I, high magnification of boxed area). Yellow arrowheads indicate a few intrafusal NMJs innervated by PGP9.5+ and Hb9::GFP+ motor axons (example boxed and shown at higher magnification in J). Scale bars: (E,F) 20 μm; (H) 200 μm (100 μm in inset); (I,J) 25 μm.
From: Shneider NA, Brown MN, Smith CA, Pickel J, Alvarez FJ.
Gamma motor neurons express distinct genetic markers at birth and require muscle spindle-derived GDNF for postnatal survival.
Neural Dev. 2009 Dec 2;4:42.
This image is from an open access article distributed under the terms of a Creative Commons Attribution License.
Sheep anti Green Fluorescent Protein antibody (4745-1051) used to assess Green Fluorescent Protein expression in Drosophila cell lysates by western blotting.
Image caption:
In all western analyses, blotting antibodies are indicated at the bottom of each panel. Fractions and the source of cells transfected with different constructs are written at the top of panels. S2 cells are derived from a macrophage-like lineage of fly embryonic cells78, and express neither Sona nor Wg10,19,33. Therefore, UAST-GFP-wg and UAST-sona-HA cDNA constructs were expressed by actin-Gal4 driver in S2 cells. HA is the preparation from cells transfected with the control UAST-HA vector. The pound signs (#) indicate the cleaved Wg fragments in the absence of Sona. These fragments may be generated by degradation during sample preparation or by some Wg-specific proteases endogenously expressed in S2 cells.g, The black arrow and the arrowhead indicate 65 and 60 kDa GFP-Wg fragments, respectively.
From:Won JH, Kim GW, Kim JY, Cho DG, Kwon B, Bae YK, Cho KO.
ADAMTS Sol narae cleaves extracellular Wingless to generate a novel active form that regulates cell proliferation in Drosophila.
Cell Death Dis. 2019 Jul 22;10(8):564.
doi: 10.1038/s41419-019-1794-8 .
This image is from an open access article distributed under the terms of a Creative Commons Attribution License.
Sheep anti green fluorescent protein antibody (4745-1051) used to lstain GFP labeled proteins in Drosophila wing discs by immunofluorescence.
Image caption:
Double knockdown of Cora and Tctp causes abnormal folding in wing disc.
Effects of RNAi by MS1096-Gal4 on wing discs. Wing discs were stained for GFP and Phal. The dotted circle and the horizontal line indicate the wing pouch and the dorsoventral boundary, respectively. MS1096-Gal4 control shows normal wing disc with preferential GFP expression in the wing pouch (A-A”’). Tctp RNAi results in slight reduction of the wing disc. Phal staining is also reduced (B-B”’).
From: Lee SR, Hong ST, Choi KW.
Regulation of epithelial integrity and organ growth by Tctp and Coracle in Drosophila.
PLoS Genet. 2020 Jun 19;16(6): e1008885.
doi: 10.1371/journal.pgen.1008885.
This image is from an open access article distributed under terms of a Creative Commons Attribution License.
Sheep anti green fluorescent protein antibody (4745-1051) used to lstain GFP labeled proteins in Drosophila wing discs by immunofluorescence.
Image caption:
Double knockdown of Cora and Tctp causes abnormal folding in wing disc.
Effects of RNAi by MS1096-Gal4 on wing discs. Wing discs were stained for GFP and Phal. The dotted circle and the horizontal line indicate the wing pouch and the dorsoventral boundary, respectively. cora RNAi reduces wing disc size. GFP staining in the hinge region is enhanced. These discs show abnormally aggregated Phal staining in some patches of wing tissues (arrows) (C-C”’). Wing discs with double RNAi for Cora and Tctp appear to be smaller than the discs with cora or Tctp single RNAi. However, most discs show bulging of wrinkled wing pouch. Phal staining is intensely accumulated in the apical or basal part of the wing pouch epithelium (arrows) (D-D”’).
From: Lee SR, Hong ST, Choi KW.
Regulation of epithelial integrity and organ growth by Tctp and Coracle in Drosophila.
PLoS Genet. 2020 Jun 19;16(6): e1008885.
doi: 10.1371/journal.pgen.1008885.
This image is from an open access article distributed under terms of a Creative Commons Attribution License.
Sheep anti Green Fluorescent Protein antibody (4745-1051) used to assess Green Fluorescent Protein expression in Drosophila wings by immunofluorescence.
Image caption:
h, I PH3 pattern in mid-3rd instar wing discs of ptc > GFP and ptc > GFP, wg-mycCTD. An arrow indicates increase in PH3 staining along the ptc region in (I).
From:Won JH, Kim GW, Kim JY, Cho DG, Kwon B, Bae YK, Cho KO.
ADAMTS Sol narae cleaves extracellular Wingless to generate a novel active form that regulates cell proliferation in Drosophila.
Cell Death Dis. 2019 Jul 22;10(8):564.
doi: 10.1038/s41419-019-1794-8 .
This image is from an open access article distributed under the terms of a Creative Commons Attribution License.
Sheep anti Green Fluorescent Protein antibody (4745-1051) used to immunostain GFP expressing cells in rat brain by immunofluorescence.
Image caption:
Overexpression of co-activators Yap1 and Taz affects cell fate, neuronal migration and cortical layering. (c) Coronal sections of transfected cortices immunostained for GFP and Tbr1, deep layer marker. (d) Quantification of Tbr1+GFP+ cells shows a reduction upon overexpression of Yap1 and Taz, compared to GFP control in CP and total. Scale bar = 50μm. Data are shown as average ± SEM, *p = 0.05, **p = 0.01, ***p = 0.001.
From: Mukhtar T, Breda J, Grison A, Karimaddini Z, Grobecker P, Iber D, Beisel C, van Nimwegen E, Taylor V.
Tead transcription factors differentially regulate cortical development.
Sci Rep. 2020 Mar 13;10(1):4625.
doi: 10.1038/s41598-020-61490-5.
This image is from an open access article distributed under terms of a Creative Commons Attribution License.
Sheep anti Green Fluorescent Protein antibody (4745-1051) used to immunostain GFP expressing cells in rat brain by immunofluorescence.
Image caption:
Overexpression of co-activators Yap1 and Taz affects cell fate, neuronal migration and cortical layering. (e) Coronal sections of transfected cortices immunostained for GFP and Ctip2, deep layer marker. (f) Quantification of Ctip2+GFP+ cells shows a reduction compared to GFP control in CP and no change in total, upon overexpression of Yap1 and Taz. IUE- in utero electroporation. Total = VZ+SVZ/IZ+CP.
From: Mukhtar T, Breda J, Grison A, Karimaddini Z, Grobecker P, Iber D, Beisel C, van Nimwegen E, Taylor V.
Tead transcription factors differentially regulate cortical development.
Sci Rep. 2020 Mar 13;10(1):4625.
doi: 10.1038/s41598-020-61490-5.
This image is from an open access article distributed under terms of a Creative Commons Attribution License.
Sheep anti Green Fluorescent Protein antibody (4745-1051) used to label GFP tagged Ihh + HHIP construct products in chick neural tube by immunofluorescence.
Image caption:
d WT and BDA1 IHH constructs were electroporated with/without HHIP to one side of the chick neural tube (HH 11-12), and the known expression regions of NKX2.2 and PAX6 in the control half are illustrated. e Overexpression of WT IHH induced expression of ventral marker NKX2.2 in the dorsal region, this effect was weaker in all IHH mutants. NKX2.2 expression was restricted to the ventral region when WT-IHH and HHIP were co-expressed. A similar pattern was observed in E95K and D100E mutations. NKX2.2 expression in the remaining three IHH mutations was abolished in the presence of HHIP. Scale bar = 100 μm. Mean fluorescence densities from experimental replicates are shown in the bar chart. f Overexpression of WT IHH suppressed expression of dorsal marker PAX6. Weaker suppression of Pax6 in mutant IHHs was observed. Co-expression of IHH and HHIP restored PAX6 expression in both WT and mutant IHH. Scale bar = 100 μm. For the bar chart in d, and f, each data point represents an independent biological replicate, bar height indicates mean and error bars indicate standard deviations. p-values are calculated with a two-sided student’s t-test.
From: Leung AOW, Poon ACH, Wang X, Feng C, Chen P, Zheng Z, To MK, Chan WCW, Cheung M, Chan D.
Suppression of apoptosis impairs phalangeal joint formation in the pathogenesis of brachydactyly type A1.
Nat Commun. 2024 Mar 12;15(1):2229.
doi: 10.1038/s41467-024-45053-0.
This image is from an open access article distributed under terms of a Creative Commons Attribution License.
Sheep anti Green Fluorescent Protein
- Product Type
- Polyclonal Antibody
- Isotype
- Polyclonal IgG
- Specificity
- Green Fluorescent Protein
Antibody Quality and Performance Guarantee
| Sheep anti Green Fluorescent Protein antibody recognizes green fluorescent protein (GFP), a ~27 kDa protein derived from the jellyfish Aequorea victoria. GFP fluoresces green (509nm) when excited by blue light (395nm) and is commonly used as a marker of gene expression. |
- Product Form
- Purified IgG - liquid
- Preparation
- Purified IgG prepared by affinity chromatography on Protein G.
- Buffer Solution
- Phosphate buffered saline
- Preservative Stabilisers
- 0.09% Sodium Azide (NaN3)
- Immunogen
- Green fluorescent protein from Aequorea victoria.
- Approx. Protein Concentrations
- IgG concentration 5.0 mg/ml
- Regulatory
- For research purposes only
- Guarantee
- 12 months from date of despatch
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.
Avoid repeated freezing and thawing as this may denature the antibody. Storage in frost-free freezers is not recommended.
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 Name | Verified | Min Dilution | Max Dilution |
|---|---|---|---|
| ELISA |  |
||
| Immunofluorescence | |
Where this product 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 product for use in their own system using the appropriate negative/positive controls.
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References for Green Fluorescent Protein antibody
-
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League, G.P. and Nam, S.C. (2011) Role of kinesin heavy chain in Crumbs localization along the rhabdomere elongation in Drosophila photoreceptor.
PLoS One. 6:e21218.
View The Latest Product References
-
Haberlandt, C. et al. (2011) Gray matter NG2 cells display multiple Ca2+-signaling pathways and highly motile processes.
PLoS One. 6: e17575. -
Srinivasan, S. et al. (2012) The receptor tyrosine phosphatase Lar regulates adhesion between Drosophila male germline stem cells and the niche.
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de Nooij, J.C. et al. (2015) The PDZ-domain protein Whirlin facilitates mechanosensory signaling in mammalian proprioceptors.
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Schlegel, P. et al. (2016) Synaptic transmission parallels neuromodulation in a central food-intake circuit.
eLife 2016;10.7554/eLife.16799 -
Gushchina, S. et al. (2018) Increased expression of colony-stimulating factor-1 in mouse spinal cord with experimental autoimmune encephalomyelitis correlates with microglial activation and neuronal loss.
Glia. 66 (10): 2108-25. -
Sagner, A. et al. (2018) Olig2 and Hes regulatory dynamics during motor neuron differentiation revealed by single cell transcriptomics.
PLoS Biol. 16 (2): e2003127. -
Won, J.H. et al. (2019) ADAMTS Sol narae cleaves extracellular Wingless to generate a novel active form that regulates cell proliferation in Drosophila.
Cell Death Dis. 10 (8): 564. -
Balaskas, N. et al. (2019) Positional Strategies for Connection Specificity and Synaptic Organization in Spinal Sensory-Motor Circuits.
Neuron. 102 (6): 1143-1156.e4. -
Zhang, R. et al. (2019) Id4 Downstream of Notch2 Maintains Neural Stem Cell Quiescence in the Adult Hippocampus.
Cell Rep. 28 (6): 1485-1498.e6. -
Mukhtar, T. et al. (2020) Tead transcription factors differentially regulate cortical development.
Sci Rep. 10 (1): 4625. -
Heath, S.L. et al. (2020) Circuit Mechanisms Underlying Chromatic Encoding in Drosophila Photoreceptors.
Curr Biol. 30 (2): 264-275.e8. -
Lee, S.R. et al. (2020) Regulation of epithelial integrity and organ growth by Tctp and Coracle in Drosophila..
PLoS Genet. 16 (6): e1008885. -
Choquet, C. et al. (2020) Nkx2-5 defines distinct scaffold and recruitment phases during formation of the murine cardiac Purkinje fiber network.
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Del Valle Rodríguez, A. et al. (2020) A network approach to analyze neuronal lineage and layer innervation in the Drosophila optic lobes.
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Poupault, C. et al. (2021) A combinatorial cis-regulatory logic restricts color-sensing Rhodopsins to specific photoreceptor subsets in Drosophila..
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Oliver, K.M. et al. (2021) Molecular correlates of muscle spindle and Golgi tendon organ afferents.
Nat Commun. 12 (1): 1451. -
Zhu, H. et al. (2022) A comprehensive temporal patterning gene network in Drosophila medulla. neuroblasts revealed by single-cell RNA sequencing.
Nat Commun. 13 (1): 1247. -
Parmigiani, E. & Giachino, C. (2022) Genetic Inactivation of Notch1 Synergizes with Loss of Trp53 to Induce Tumor Formation in the Adult Mouse Forebrain.
Cancers (Basel). 14 (21): 5409. -
Zhang, Y. et al. (2023) Notch-dependent binary fate choice regulates the Netrin pathway to control axon guidance of Drosophila visual projection neurons.
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Liau, E.S. et al. (2023) Single-cell transcriptomic analysis reveals diversity within mammalian spinal motor neurons.
Nat Commun. 14 (1): 46. -
Zhang, Y. et al. (2023) Axon targeting of Drosophila medulla projection neurons requires diffusible Netrin and is coordinated with neuroblast temporal patterning.
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Klima, M.L. et al. (2023) Anti-inflammatory effects of hunger are transmitted to the periphery via projection-specific AgRP circuits
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Hoang, P.T. et al. (2018) Subtype Diversification and Synaptic Specificity of Stem Cell-Derived Spinal Interneurons.
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Mukhtar, T. et al. (2022) Temporal and sequential transcriptional dynamics define lineage shifts in corticogenesis.
EMBO J. 41 (24): e111132. -
Leung, A.O.W. et al. (2024) Suppression of apoptosis impairs phalangeal joint formation in the pathogenesis of brachydactyly type A1.
Nat Commun. 15 (1): 2229.
Further Reading
-
Adams, K.L. et al. (2015) Foxp1-mediated programming of limb-innervating motor neurons from mouse and human embryonic stem cells.
Nat Commun. 6: 6778.
- RRID
- AB_619712
- UniProt
- P42212
- GO Terms
- GO:0006091 generation of precursor metabolites and energy
- GO:0008218 bioluminescence
- GO:0018298 protein-chromophore linkage
4745-1051
163365
1710
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