Purified anti-TP63 Antibody anti-p63 - W15093A,BioLegend,687202

Application Notes: This clone predominantly recognizes ?N-p63, and weakly crosses react with TA-p63. Both ?N-p63 and TA-p63 have multiple isoforms, the largest isoforms are 66kD and 77kD respectively. This antibody recognizes more than one isoform of ?N-p63.

Host

Mouse

Reactivity

Human

Application

WB -Quality testedChIP- Verified

Platform ID

BAB327854492

BioLegend

Headquarters

8999 BioLegend Way San Diego, CA 92121 United States

Contact

Tel: 1-858-455-9588
Fax: +49 (4131) 7023913

Email:

Product Specifications
Scientific Background

Specifications

NamePurified anti-TP63 Antibody anti-p63 - W15093A
Cat. No.687202
HostMouse
RRIDAB_2616941 (BioLegend Cat. No. 687202)
IsotypeMouse IgG2b, κ
ReactivityHuman
ApplicationWB -Quality testedChIP- Verified
ClonalityMonoclonal
Clone NumberW15093A
Concentration0.5 mg/ml
TargetTP63
ImmunogenPartial human TP63 recombinant protein (1-250 a.a.) expressed inE. coli.
PurityThe antibody was purified by affinity chromatography.
FormulationPhosphate-buffered solution, pH 7.2, containing 0.09% sodium azide.
StorageThe antibody solution should be stored undiluted between 2°C and 8°C.
Regulatory StatusResearch Use Only

Scientific Background

TP63 is a p53-related gene and shares similar domain organization with p53 and p73. Full length TP63 contains a N-terminal transactivation domain, a central DNA binding domain, and a C-terminal oligomerization domain responsible for the formation of a homotetramer. TP63 have several isoforms produced by alternative splicing. Most of the isoforms contain the DNA binding domain, but differ in their transactivation and oligomerization domains. The transactivation domain is present in the transcriptional active isoforms (TA-p63) and is absent in the truncated isoforms (ΔN -p63). TP63 is expressed in keratinocyte stem cells and is essential for the morphogenesis and development of ectodermal, orofacial, and limb tissues. TP63 deficient mice die soon after birth with skin and limb developmental defects.

Category Paths

Request a product

Please provide the required information below so that we can quickly source your products.