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Merck

G9293

Sigma-Aldrich

Anti-GAL4, Activation domain antibody produced in rabbit

~1.0 mg/mL, affinity isolated antibody, buffered aqueous solution

Sinónimos:

Anti-Galactose 4

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About This Item

MDL number:
UNSPSC Code:
12352203
NACRES:
NA.56

biological source

rabbit

Quality Level

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

form

buffered aqueous solution

concentration

~1.0 mg/mL

technique(s)

western blot: 0.5 μg/mL using GAL4-AD fusion protein in Saccharomyces cerevisiae extract

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

General description

GAL4 protein is an 881 amino acid transcription factor containing an independent N-terminal DNA binding (147 amino acids) and C-terminal activator domains. It is a regulatory gene that belongs to GAL gene family. It is a component of yeast two hybrid system, where GAL 4 DNA-BD is fused to protein X (bait) and GAL4 activation domain is fused to protein Y (prey).
Useful in the study of protein:protein interaction studies. GAL4 DNA activation domain fusion proteins.

Immunogen

Synthetic peptide corresponding to amino acids of Saccharomyces cerevisiae GAL4 protein.

Application

Anti-GAL4, Activation domain antibody produced in rabbit has been used in western blotting.

Biochem/physiol Actions

GAL4 induces the genes that are responsible for regulation of galactose metabolism in saccharomyces cerevisiae. GAL4 protein is widely used for studying transcriptional activation in eukaryotes. The yeast two hybrid system is widely used to study to discover protein− protein interactions (PPIs) and protein−DNA interactions.

Physical form

The product is provided as a solution of affinity isolated antibody in 0.01 M phosphate buffered saline, pH 7.4, containing 1% bovine serum albumin and 15 mM sodium azide as a preservative.

Storage and Stability

For continuous use, store at 2-8 °C for up to one month. For extended storage, freeze in working aliquots. Repeated freezing and thawing is not recommended. Storage in “frost-free” freezers is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilution samples should be discarded if not used within 12 hours.

Disclaimer

Unless otherwise stated in our catalog, 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.

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Storage Class

10 - Combustible liquids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Visite la Librería de documentos

Yeast Gal4: a transcriptional paradigm revisited
Traven A, et al.
EMBO Reports, 7(5), 496-499 (2006)
Alessandro Berto et al.
EMBO reports, 19(5) (2018-04-11)
Cenp-F is a multifaceted protein implicated in cancer and developmental pathologies. The Cenp-F C-terminal region contains overlapping binding sites for numerous proteins that contribute to its functions throughout the cell cycle. Here, we focus on the nuclear pore protein Nup133
Temperature-sensitive Mutations Made Easy Generating Conditional Mutations Using TS-inteins That Function Within Different Temperature Ranges
Tan G, et al.
Genetics, 62(1-2), 291-304 (2009)
Lidia Hurtado et al.
Plant molecular biology, 62(1-2), 291-304 (2006-07-18)
Arabidopsis thaliana BRAHMA (BRM, also called AtBRM) is a SNF2 family protein homolog of Brahma, the ATPase of the Drosophila SWI/SNF complex involved in chromatin remodeling during transcription. Here we show that, in contrast to its Drosophila counterpart, BRM is
Yeast two-hybrid, a powerful tool for systems biology
Bruckner A, et al.
International Journal of Molecular Sciences, 10(6), 2763-2788 (2009)

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