ARG44755

anti-p63 antibody

anti-p63 antibody for IHC-Formalin-fixed paraffin-embedded sections,Immunoprecipitation,Western blot and Human

Overview

Product Description Mouse Monoclonal antibody recognizes p63
Tested Reactivity Hu
Tested Application IHC-P, IP, WB
Host Mouse
Clonality Monoclonal
Isotype IgG2b
Target Name p63
Antigen Species Human
Conjugation Un-conjugated
Alternate Names p63; Tumor protein p73-like; B(p51A); AIS; p53CP; p73L; p73H; p40; EEC3; TP63; NBP; Chronic ulcerative stomatitis protein; TP53CP; CUSP; B(p51B); TP73L; p51; Transformation-related protein 63; Keratinocyte transcription factor KET; SHFM4; TP53L; RHS; LMS; Tumor protein 63; OFC8; KET

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-P1 µg/mL
IP10 µg/mL
WB1 µg/mL
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.

Properties

Form Liquid
Purification Protein A purification
Buffer PBS with 0.09% sodium azide
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 8626 Human TP63

Swiss-port # Q9H3D4 Human Tumor protein 63

Gene Symbol TP63
Gene Full Name tumor protein p63
Background This gene encodes a member of the p53 family of transcription factors. An animal model, p63 -/- mice, has been useful in defining the role this protein plays in the development and maintenance of stratified epithelial tissues. p63 -/- mice have several developmental defects which include the lack of limbs and other tissues, such as teeth and mammary glands, which develop as a result of interactions between mesenchyme and epithelium. Mutations in this gene are associated with ectodermal dysplasia, and cleft lip/palate syndrome 3 (EEC3); split-hand/foot malformation 4 (SHFM4); ankyloblepharon-ectodermal defects-cleft lip/palate; ADULT syndrome (acro-dermato-ungual-lacrimal-tooth); limb-mammary syndrome; Rap-Hodgkin syndrome (RHS); and orofacial cleft 8. Both alternative splicing and the use of alternative promoters results in multiple transcript variants encoding different proteins. Many transcripts encoding different proteins have been reported but the biological validity and the full-length nature of these variants have not been determined. [provided by RefSeq, Jul 2008]
Function May be involved in the generation of reactive oxygen species (ROS). Has low NADPH-dependent beta-naphthoquinone reductase activity, with a preference for 1,2-beta-naphthoquinone over 1,4-beta-naphthoquinone. Has low NADPH-dependent diamine reductase activity (in vitro). [UniProt]
PTM May be sumoylated.
Ubiquitinated. Polyubiquitination involves WWP1 and leads to proteasomal degradation of this protein.

Images (3) Click the Picture to Zoom In

  • ARG44755 anti-p63 antibody IHC-P image

    Immunohistochemistry: Human prostate stained with ARG44755 anti-p63 antibody at 1 µg/mL dilution.

  • ARG44755 anti-p63 antibody WB image

    Western blot: A431 stained with ARG44755 anti-p63 antibody at 1 µg/mL dilution.

  • ARG44755 anti-p63 antibody IP image

    Immunoprecipitation: A431 lysate immunoprecipitated with 2.5 µg of ARG44755 anti-p63 antibody.