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
- Purified IgG prepared by affinity chromatography on Protein G.
- Buffer Solution
- Phosphate buffered saline
- Preservative Stabilisers
- 0.09% Sodium Azide (NaN3)
- Green fluorescent protein from Aequorea victoria.
- Approx. Protein Concentrations
- IgG concentration 5.0 mg/ml
- Store at +4oC or at -20oC if preferred.
Storage in frost-free freezers is not recommended.
This product should be stored undiluted. Avoid repeated freezing and thawing as this may denature the antibody. Should this product contain a precipitate we recommend microcentrifugation before use.
- 12 months from date of despatch
- GO Terms
generation of precursor metabolites and energy
- 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.
Applications of Green Fluorescent Protein antibody
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.
Copyright © 2020 Bio-Rad Antibodies (formerly AbD Serotec)
Secondary Antibodies Available
Useful Reagents Available
Application Based External Images
Product Specific References
References for Green Fluorescent Protein antibody
Collins, R.T. et al. (2010) MAZe: a tool for mosaic analysis of gene function in zebrafish.
Nat Methods. 7: 219-23.
Wu, L. et al. (2011) Properties of a distinct subpopulation of GABAergic commissural interneurons that are part of the locomotor circuitry in the neonatal spinal cord.
J Neurosci. 31 (13): 4821-33.
Knipe, L. et al. (2010) A revised model for the secretion of tPA and cytokines from cultured endothelial cells.
Blood. 116: 2183-91.
Shneider, N.A. et al. (2009) Gamma motor neurons express distinct genetic markers at birth and require muscle spindle-derived GDNF for postnatal survival.
Neural Dev. 4: 42.
Soza-Ried, C. et al. (2008) Maintenance of thymic epithelial phenotype requires extrinsic signals in mouse and zebrafish.
J Immunol. 181: 5272-7.
Lopez, K.A. et al. (2011) Convection-enhanced delivery of topotecan into a PDGF-driven model of glioblastoma prolongs survival and ablates both tumor-initiating cells and recruited glial progenitors.
Cancer Res. 71: 3963-71.
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.
Siembab, V.C. et al. (2010) Target selection of proprioceptive and motor axon synapses on neonatal V1-derived Ia inhibitory interneurons and Renshaw cells.
J Comp Neurol. 518: 4675-701.
Srinivasan, S. et al. (2012) The receptor tyrosine phosphatase Lar regulates adhesion between Drosophila male germline stem cells and the niche.
Development. 139: 1381-90.
Haberlandt, C. et al. (2011) Gray matter NG2 cells display multiple Ca2+-signaling pathways and highly motile processes.
PLoS One. 6: e17575.
Cheung, L.S. et al. (2013) Dynamic model for the coordination of two enhancers of broad by EGFR signaling.
Proc Natl Acad Sci U S A. 110: 17939-44.
Li, X. et al. (2013) Temporal patterning of Drosophila medulla neuroblasts controls neural fates.
Nature. 498: 456-62.
Behnia, R. et al. (2014) Processing properties of ON and OFF pathways for Drosophila motion detection.
Nature. 512: 427-30.
de Nooij, J.C. et al. (2015) The PDZ-domain protein Whirlin facilitates mechanosensory signaling in mammalian proprioceptors.
J Neurosci. 35 (7): 3073-84.
Scotti, M. et al. (2015) A Hoxa13:Cre mouse strain for conditional gene manipulation in developing limb, hindgut, and urogenital system.
Genesis. 53 (6): 366-76.
Sun, G.J. et al. (2015) Latent tri-lineage potential of adult hippocampal neural stem cells revealed by Nf1 inactivation.
Nat Neurosci. 18 (12): 1722-4.
Schlegel, P. et al. (2016) Synaptic transmission parallels neuromodulation in a central food-intake circuit.
Crouch, E.E. et al. (2015) Regional and stage-specific effects of prospectively purified vascular cells on the adult V-SVZ neural stem cell lineage.
J Neurosci. 35 (11): 4528-39.
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.
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.
Del Valle Rodríguez, A. et al. (2020) A network approach to analyze neuronal lineage and layer innervation in the Drosophila optic lobes.
PLoS One. 15 (2): e0227897.
Choquet, C. et al. (2020) Nkx2-5 defines distinct scaffold and recruitment phases during formation of the murine cardiac Purkinje fiber network.
Nat Commun. 11 (1): 5300.
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.