TBX3 Polyclonal Antibody

    • Catalog No.:YT4571
    • Applications:WB;ELISA
    • Reactivity:Human;Mouse;Rat
      • Target:
      • TBX3
      • Fields:
      • >>Signaling pathways regulating pluripotency of stem cells
      • Gene Name:
      • TBX3
      • Protein Name:
      • T-box transcription factor TBX3
      • Human Gene Id:
      • 6926
      • Human Swiss Prot No:
      • O15119
      • Mouse Swiss Prot No:
      • P70324
      • Immunogen:
      • The antiserum was produced against synthesized peptide derived from human TBX3. AA range:301-350
      • Specificity:
      • TBX3 Polyclonal Antibody detects endogenous levels of TBX3 protein.
      • Formulation:
      • Liquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
      • Source:
      • Polyclonal, Rabbit,IgG
      • Dilution:
      • WB 1:500 - 1:2000. ELISA: 1:5000. Not yet tested in other applications.
      • Purification:
      • The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
      • Concentration:
      • 1 mg/ml
      • Storage Stability:
      • -15°C to -25°C/1 year(Do not lower than -25°C)
      • Other Name:
      • TBX3;T-box transcription factor TBX3;T-box protein 3
      • Observed Band(KD):
      • 79kD
      • Background:
      • This gene 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 protein is a transcriptional repressor and is thought to play a role in the anterior/posterior axis of the tetrapod forelimb. Mutations in this gene cause ulnar-mammary syndrome, affecting limb, apocrine gland, tooth, hair, and genital development. Alternative splicing of this gene results in three transcript variants encoding different isoforms; however, the full length nature of one variant has not been determined. [provided by RefSeq, Jul 2008],
      • Function:
      • disease:Defects in TBX3 are the cause of ulnar-mammary syndrome (UMS) [MIM:181450]. UMS is characterized by ulnar ray defects, obesity, hypogenitalism, delayed puberty, hypoplasia of nipples and apocrine glands.,function:Transcriptional repressor involved in developmental processes. Probably plays a role in limb pattern formation.,similarity:Contains 1 T-box DNA-binding domain.,tissue specificity:Widely expressed.,
      • Subcellular Location:
      • Nucleus .
      • Expression:
      • Widely expressed.
      • Products Images
      • Western Blot analysis of KB cells using TBX3 Polyclonal Antibody diluted at 1:1000
      • Western blot analysis of mouse-kidney mouse-brain KB 293T lysis using TBX3 antibody. Antibody was diluted at 1:1000