Twist (TWIST1) (NM_000474) Human Recombinant Protein
Product Specifications
Background
This gene encodes a basic helix-loop-helix (bHLH) transcription factor that plays an important role in embryonic development. The encoded protein forms both homodimers and heterodimers that bind to DNA E box sequences and regulate the transcription of genes involved in cranial suture closure during skull development. This protein may also regulate neural tube closure, limb development and brown fat metabolism. This gene is hypermethylated and overexpressed in multiple human cancers, and the encoded protein promotes tumor cell invasion and metastasis, as well as metastatic recurrence. Mutations in this gene cause Saethre-Chotzen syndrome in human patients, which is characterized by craniosynostosis, ptosis and hypertelorism. [provided by RefSeq, Jul 2020]
Synonyms
ACS3; bHLHa38; BPES2; BPES3; CRS; CRS1; CSO; SCS; SWCOS; TWIST
Gene ID
7291
UniProt
Q15672
Accession Number mRNA
NM_000474
Chromosomal Location
7p21.1
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
Druggable Genome
Molecular Weight
20.8 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
TWIST1
Species
Human
Protein ID
NP_000465
Overview
Recombinant protein of human twist homolog 1 (Drosophila) (TWIST1)
Gene ID URL
https://www.ncbi.nlm.nih.gov/gene/7291
Uniprot URL
https://www.uniprot.org/uniprot/Q15672
Accession Number mRNA URL
https://www.ncbi.nlm.nih.gov/nuccore/NM_000474
Protein ID Link
https://www.ncbi.nlm.nih.gov/nuccore/NP_000465
Curated Selection
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