PIPA526389

TBX1 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA526389-Each-of-1 In Stock ₹ 49,083.50

PIPA526389 - Each of 1

₹ 49,083.50

In Stock

Quantity

1

Base Price: ₹ 49,083.50

GST (18%): ₹ 8,835.03

Total Price: ₹ 57,918.53

Antigen

TBX1

Classification

Polyclonal

Conjugate

Unconjugated

Gene

TBX1

Gene Alias

brachyury; CAFS; CATCH22; CTHM; DGCR; DGS; DORV; LOW QUALITY PROTEIN: T-box transcription factor TBX1; T-box 1; T-box 1 transcription factor C; T-box protein 1; T-box transcription factor 1; T-box transcription factor TBX1; T-box transcription factor TBX1; LOW QUALITY PROTEIN: T-box transcription factor TBX1; Tbx1; TBX1C; Testis-specific T-box protein; TGA; VCF; VCFS

Host Species

Rabbit

Purification Method

Antigen affinity chromatography, Protein A

Regulatory Status

RUO

Gene ID (Entrez)

6899

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

Applications

Immunocytochemistry, Immunohistochemistry (Paraffin), Western Blot

Concentration

0.5 mg/mL

Formulation

PBS with 0.09% sodium azide

Gene Accession No.

O43435

Gene Symbols

TBX1

Immunogen

KLH conjugated synthetic peptide between 327-356 amino acids from the C-terminal region of human TBX1

Quantity

400 μL

Primary or Secondary

Primary

Target Species

Human

Product Type

Antibody

Isotype

Ig

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Description

  • TBX1 is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box
  • T-box genes encode transcription factors involved in the regulation of developmental processes
  • This gene product shares 98% amino acid sequence identity with the mouse ortholog
  • DiGeorge syndrome (DGS)/velocardiofacial syndrome (VCFS), a common congenital disorder characterized by neural-crest-related developmental defects, has been associated with deletions of chromosome 22q11.2, where this gene has been mapped
  • Studies using mouse models of DiGeorge syndrome suggest a major role for this gene in the molecular etiology of DGS/VCFS
  • Several alternatively spliced transcript variants encoding different isoforms have been described for this gene.