TBX3 rabbit pAb

TBX3 rabbit pAb

AO-06-ES7348-100

TBX3 rabbit pAb 100μL

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Antibody Product Overview

ELK.NoES7348
Product nameTBX3 rabbit pAb
ReactivityHuman;Mouse;Rat
ApplicationsWB;ELISA
Other nameTBX3; T-box transcription factor TBX3; T-box protein 3
Size100μL
Unit price ($)248
Human gene ID6926
Human Swiss-ProtO15119
SourceRabbit
IsotypeIgG
TargetTBX3
Fields>>Signaling pathways regulating pluripotency of stem cells
Gene nameTBX3
Protein nameT-box transcription factor TBX3
Human gene linkView Human Gene
Human Swiss linkView Human Swiss-Prot
Mouse gene ID21386
Mouse gene linkView Mouse Gene
Mouse Swiss-ProtP70324
Mouse Swiss linkView Mouse Swiss-Prot
Rat gene ID353305
Rat gene linkView Rat Gene
Rat Swiss-ProtQ7TST9
Rat Swiss linkView Rat Swiss-Prot
ImmunogenThe antiserum was produced against synthesized peptide derived from human TBX3. AA range:301-350
SpecificityTBX3 Polyclonal Antibody detects endogenous levels of TBX3 protein.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
ClonalityPolyclonal
DilutionWestern Blot: 1/500 - 1/2000. ELISA: 1/5000. Not yet tested in other applications.
PurificationThe antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
Concentration1 mg/ml
Storage stability-20°C/1 year
Molecular Weight (Da)
Observed band (KD)79kD
BackgroundThis 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],
Functiondisease: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 locationNucleus .
ExpressionWidely expressed.

Additional Images

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Western Blot analysis of KB cells using TBX3 Polyclonal Antibody diluted at 1:1000
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Western blot analysis of mouse-kidney mouse-brain KB 293T lysis using TBX3 antibody. Antibody was diluted at 1:1000
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: AO-06-ES7348-100
: 10 Produits
Hurry! only 10 items left in stock.

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