SKU: WM0438 Categories: ,

TBX5 Monoclonal Antibody

Price range: $268.00 through $328.00

SKU: WM0438-50
Enter the quantity you would like, or drag the panel to find the quantity and price that best for you
Bulk QuoteAuthorize OEM & ODM

Product details

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 gene is closely linked to related family member T-box 3 (ulnar mammary syndrome) on human chromosome 12. The encoded protein may play a role in heart development and specification of limb identity. Mutations in this gene have been associated with Holt-Oram syndrome, a developmental disorder affecting the heart and upper limbs. Several transcript variants encoding different isoforms have been described for this gene. [provided by RefSeq, Jul 2008],

Specifications

Size50μL/100μL
TargetTBX5
ReactivityHuman
ApplicationsWB, ELISA
MW(Calculated)58kD
MW(Observed)
Host SpeciesMouse
Isotype
Conjugate/ModificationUnmodified
Recommended Dilution RatioWB 1:500-1:2000; ELISA 1:10000; Not yet tested in other applications.
FormulationLiquid in PBS containing 50% glycerol, 0.5% BSA and 0.02% sodium azide.
PurificationAffinity purification
Storage-15°C to -25°C/1 year(Do not lower than -25°C)
Concentration
ClonalityMonoclonal
Clone Number13A2
ImmunogenPurified recombinant fragment of TBX5 expressed in E. Coli.
SpecificityTBX5 Monoclonal Antibody detects endogenous levels of TBX5 protein.
Gene NameTBX5
Protein NameT-box transcription factor TBX5
Other NameTBX5; / T-box transcription factor TBX5; / T-box protein 5
SpeciesHuman
Gene ID6910
UniprotQ99593,
Species.1Mouse
Gene ID.1
Uniprot.1P70326
Species.2
Gene ID.2
Uniprot.2
Cellular LocalizationNucleus . Cytoplasm . Shuttles between the cytoplasm and the nucleus. Acetylation at Lys-339 promotes nuclear retention. .
Tissue ExpressionLung,Spleen,
Signaling_pathway
Research Areas
FunctionDisease:Defects in TBX5 are the cause of Holt-Oram syndrome (HOS) [MIM:142900]. HOS is a developmental disorder affecting the heart and upper limbs. It is characterized by thumb anomaly and atrial septal defects.,Function:Involved in the transcriptional regulation of genes required for mesoderm differentiation. Probably plays a role in limb pattern formation.,similarity:Contains 1 T-box DNA-binding domain.,
Please login to post questions
Back to Top
Product has been added to your cart