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11814460001

Roche

Anti-GFP

from mouse IgG1κ (clones 7.1 and 13.1)

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Synonym(s):
anti-green fluorescent protein

biological source

mouse

Quality Level

conjugate

unconjugated

antibody form

purified immunoglobulin

antibody product type

primary antibodies

clone

13.1, monoclonal
7.1, monoclonal

assay

>90% (HPLC)

form

lyophilized

packaging

pkg of 200 μg

manufacturer/tradename

Roche

isotype

IgG1κ

storage temp.

2-8°C

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This Item
SAB4200681G6539AB16901
vibrant-m

11814460001

Anti-GFP

antibody form

purified immunoglobulin

antibody form

purified antibody

antibody form

ascites fluid

antibody form

purified immunoglobulin

conjugate

unconjugated

conjugate

-

conjugate

unconjugated

conjugate

-

biological source

mouse

biological source

mouse

biological source

mouse

biological source

chicken

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

-

isotype

IgG1κ

isotype

IgG1

isotype

IgG1

isotype

-

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General description

Green Fluorescent Protein (GFP) is a spontaneously fluorescent 27kDa protein originally isolated from the jellyfish Aequorea victoria. The molecular cloning of the GFP gene and its subsequent expression in heterologous systems has established GFP as a valuable reporter molecule for in vivo visualization of gene expression events in a wide variety of cell types and organisms. Since, GFP requires no additional substrates or cofactors, GFP′s green fluorescence can be easily detected using blue or UV light after expression in either prokaryotic or eukaryotic cells. In addition, several mutant forms of GFP with unique spectral properties (e.g., enhanced fluorescence signal and shifts in excitation and emission spectra) have been reported.
Mixture of two high-affinity monoclonal antibodies selected for their performance in detection of GFP and GFP fusion proteins.

Specificity

Subtype: Both clones are Mouse IgG1κ

Application

Monoclonal antibody for detection of both wild-type and mutant forms of GFP or GFP fusions using:
  • Immunoprecipitation
  • Western blots
  • Immunostaining

Features and Benefits

Contents
Mixture of two monoclonal antibodies, supplied as a white lyophilizatecontaining 200μg of total Anti-GFP IgG.
Anti-GFP is a mixture of two clones (7.1 and 13.1).

Quality

Anti-GFP is tested for functionality and purity relative to a reference standard to confirm the quality of each new reagent preparation.
Purity: Both Anti-GFP mouse monoclonal antibodies (Clones 7.1 and 13.1) are >95% pure as determined by SDS-PAGE and ion-exchange HPLC analyses.

Preparation Note

Working concentration: Working concentration of antibody depends on application and substrate.
The following concentrations should be taken as a guideline:
  • Western blot: 1:1000 dilution
  • Immunoprecipitation: 2 to 10 μg

Storage conditions (working solution): -15 to -25 °C

Reconstitution

Add 500 μl double distilled water to a final concentration of 0.4 mg/ml.
Rehydrate on ice for 30 minutes.

Legal Information

This product is sold under license from Columbia University. Rights to use this product are limited to research use only. No other rights are conveyed. Inquiry into the availability of a license to broader rights or the use of this product for commercial purposes should be directed to Columbia Innovation Enterprise, Columbia University, Engineering Terrace - Suite 363, new York, New York 10027.

Storage Class

13 - Non Combustible Solids

wgk_germany

WGK 1

flash_point_f

does not flash

flash_point_c

does not flash


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Ward W.W, et al.
Photochemistry and Photobiology, 31, 611-615 (1980)
Chalfie M, et al.
Science, 263, 802-805 (1994)
Prasher D C, et al.
Gene, 111, 229-233 (1992)
Chi C Wong et al.
Blood, 118(16), 4305-4312 (2011-08-02)
Shwachman-Diamond syndrome (SDS), a recessive leukemia predisposition disorder characterized by bone marrow failure, exocrine pancreatic insufficiency, skeletal abnormalities and poor growth, is caused by mutations in the highly conserved SBDS gene. Here, we test the hypothesis that defective ribosome biogenesis
Cormack B P, et al.
Gene, 173, 33-38 (1996)

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