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Merck

G6539

Monoclonal Anti-Green Fluorescent Protein (GFP) antibody produced in mouse

clone GFP-20, ascites fluid

Synonyme(s) :

GFP Antibody - Monoclonal Anti-Green Fluorescent Protein (GFP) antibody produced in mouse, Gfp Antibody Sigma, Gfp Monoclonal Antibody

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A propos de cet article

UNSPSC Code:
12352203
NACRES:
NA.46
MDL number:
Conjugate:
unconjugated
Clone:
GFP-20, monoclonal
Application:
dot blot
indirect ELISA
western blot
Technique(s):
dot blot: suitable
indirect ELISA: suitable
western blot: 1:2,000 using purified recombinant GFP preparation
Citations:
170
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Nom du produit

Monoclonal Anti-Green Fluorescent Protein (GFP) antibody produced in mouse, clone GFP-20, ascites fluid

biological source

mouse

conjugate

unconjugated

antibody form

ascites fluid

antibody product type

primary antibodies

clone

GFP-20, monoclonal

mol wt

antigen 27 kDa

contains

15 mM sodium azide

packaging

antibody small pack of 25 μL

technique(s)

dot blot: suitable
indirect ELISA: suitable
western blot: 1:2,000 using purified recombinant GFP preparation

isotype

IgG1

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Quality Level

Application

Monoclonal Anti-Green Fluorescent Protein (GFP) antibody is suitable for use in western blot and ChIP assays.
Monoclonal Anti-Green Fluorescent Protein (GFP) recognizes GFP (27 kDa) using immunoblotting, dot blot, immunoprecipitation, immunocytochemistry, immunofluorescence, chromatin immunoprecipitation and enzyme linked immunosorbent assay (ELISA). The antibody reacts with fusion proteins expressed by prokaryotes expression vectors.

Disclaimer

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

General description

Monoclonal Anti-Green Fluorescent Protein (GFP) (mouse IgG1 isotype) is derived from the GFP-20 hybridoma produced by the fusion of mouse myeloma cells and splenocytes from a BALB/c mouse immunized with a GFP tagged fusion protein. GFP is a 27 kDa (238 amino acid) protein, derived from the bioluminescent jellyfish Aequorea victoria, in which light is produced when energy is transferred from the Ca2+-activated photoprotein aequorin to GFP. GFP is a unique tool to monitor dynamic processes in a variety of living cells or organisms. When expressed in either eukaryotic or prokaryotic cells and illuminated by blue or UV light, GFP yields a bright green fluorescence. Light-stimulated GFP fluorescence is species-independent and a fluorescence has been reported from many different types of GFP-expressing hosts, including microbes, invertebrates, vertebrates and plants. Exogenous substrates and cofactors are not required for the fluorescence of GFP, since GFP autocatalytically forms a fluorescent pigment from natural amino acids present in the nascent protein. GFP signals can be quantified by flow cytometry, confocal scanning laser microscopy, and fluorometric assays. Indeed, many recombinant proteins have been engineered with GFP tags to facilitate the detection, isolation and purification of the proteins.
The Green Fluorescent Protein (GFP) is derived from the jellyfish Aequorea Victoria and is often used as a gene expression marker. Thus, antibodies to GFP can facilitate the detection and analysis of GFP labeled nucleic acids and proteins. Monoclonal Anti-Green Fluorescent Protein (GFP) antibody is specific for GFP and GFP-labeled biomolecules.

Immunogen

GFP tagged fusion protein
GFP tagged fusion protein.

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Classe de stockage

12 - Non Combustible Liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


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Consulter la Bibliothèque de documents

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Dieckmann R, et al.
Molecular Biology of the Cell, 21(9), 1505-1518 (2010)
Justin M O'Sullivan et al.
Nature genetics, 36(9), 1014-1018 (2004-08-18)
Mechanistic analysis of transcriptional initiation and termination by RNA polymerase II (PolII) indicates that some factors are common to both processes. Here we show that two long genes of Saccharomyces cerevisiae, FMP27 and SEN1, exist in a looped conformation, effectively
Ca2+-dependent monomer and dimer formation switches CAPRI Protein between Ras GTPase-activating protein (GAP) and RapGAP activities
Dai Y, et al.
The Journal of Biological Chemistry, 286(22), 19905-19916 (2011)
Enhanced stability of heterologous proteins by supramolecular self-assembly
Park JS, et al.
Applied Microbiology and Biotechnology, 75(2), 347-355 (2007)
Glucagon-like peptide 1 receptor activation regulates cocaine actions and dopamine homeostasis in the lateral septum by decreasing arachidonic acid levels
Reddy IA, et al.
Translational Psychiatry, 6(5), e809-e809 (2016)

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