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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

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