GRHL2 (NM_024915) Human Recombinant Protein
Product Specifications
Background
The protein encoded by this gene is a transcription factor that can act as a homodimer or as a heterodimer with either GRHL1 or GRHL3. Defects in this gene are a cause of non-syndromic sensorineural deafness autosomal dominant type 28 (DFNA28) .[provided by RefSeq, Mar 2009]
Overview
Recombinant protein of human grainyhead-like 2 (Drosophila) (GRHL2)
Synonyms
BOM; DFNA28; ECTDS; PPCD4; TFCP2L3
Gene ID
79977
UniProt
Q6ISB3
Accession Number mRNA
NM_024915
Chromosomal Location
8q22.3
Expression System
HEK293T
Tag
C-Myc/DDK
Concentration
>50 ug/mL as determined by microplate BCA method
Purity
> 80% as determined by SDS-PAGE and Coomassie blue staining
Form
Liquid
Buffer
25 mM Tris.HCl, pH 7.3, 100 mM glycine, 10% glycerol
Function
Transcription Factors
Molecular Weight
70.9 kDa
Storage Conditions
Stable for 1 year at -20°C or below from date of shipment. For maximum recovery of product, centrifuge the original vial after thawing and opening the cap. For long-term storage, aliquot and store at -20°C or below. Avoid repeated freeze-thaw cycles.
Symbol
GRHL2
Species
Human
Protein ID
NP_079191
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/79977
Uniprot URL
https://www.uniprot.org/uniprot/Q6ISB3
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_024915
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_079191
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