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TWST1 Polyclonal Antibody

Polyclonal antibody

Specification

BYab-07769

  • 50UL $180 100UL $255
  • Delivery: In Stock

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Product introduction>

Host
Reactiveness
Use
Molecular weight (DA)
22kD
Immunogen
Synthesized peptide derived from part region of human protein
Specificity
TWST1 Polyclonal Antibody detects endogenous levels of protein.
Source
Formulation
Liquid in PBS containing 50% glycerol, and 0.02% sodium azide.
Dilution rate
WB 1:500-2000 ELISA 1:5000-20000
Purification process (Immunogen)
The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration
1 mg/ml
Background
Basic helix-loop-helix (bHLH) transcription factors have been implicated in cell lineage determination and differentiation. The protein encoded by this gene is a bHLH transcription factor and shares similarity with another bHLH transcription factor, Dermo1. The strongest expression of this mRNA is in placental tissue; in adults, mesodermally derived tissues express this mRNA preferentially. Mutations in this gene have been found in patients with Saethre-Chotzen syndrome. [provided by RefSeq, Jul 2008],
Function
disease:Defects in TWIST1 are a cause of Saethre-Chotzen syndrome (SCS) [MIM:101400]; also known as acrocephalosyndactyly type 3 (ACS3). SCS is a craniosynostosis syndrome characterized by coronal synostosis, brachycephaly, low frontal hairline, facial asymmetry, hypertelorism, broad halluces, and clinodactyly.,disease:Defects in TWIST1 are the cause of craniosynostosis type 1 (CRS1) [MIM:123100]. Craniosynostosis consists of premature fusion of one or more cranial sutures, resulting in an abnormal head shape.,disease:Defects in TWIST1 are the cause of Robinow-Sorauf syndrome (RSS) [MIM:180750]; also known as craniosynostosis-bifid hallux syndrome. RSS is an autosomal dominant defect characterized by minor skull and limb anomalies which is very similar to Saethre-Chotzen syndrome.,function:Probable transcription factor, which seems to be involved in the negative regulation of cellular de
Gene Name
TWIST1 BHLHA38 TWIST
Protein name
Twist-related protein 1 (Class A basic helix-loop-helix protein 38) (bHLHa38) (H-twist)
Abbreviation
TWST1
Other name
Fields
>>Proteoglycans in cancer
Human gene ID
7291
Human protein sequence Database
Q15672
Mouse gene ID
Mouse protein sequence database
P26687
Rat gene ID
Rat protein sequence database
Cellular localization
Nucleus.
Tissue expression
Subset of mesodermal cells.
Storage
-20°C/1 year

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Procedure

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TWST1 Polyclonal Antibody

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