Purified anti-TFAP2A Antibody, TFAP2A, W20235D,BioLegend,634351

For use of this antibody (clone W20235D) in immunohistochemistry on formalin-fixed paraffin embedded tissue (IHC-P), antigen retrieval with Tris-EDTA pH 9.0 or Citrate Buffer, 10X (Cat. No. 420902) is recommended.For use of this antibody (clone W20235D) in immunocytochemistry (ICC), fixation with either Fixation Buffer (Cat. No. 420801) followed by permeabilization with 0.5% Triton-X or 100% ice-cold methanol is recommended.For use of this antibody (clone W20235D) in intracellular flow cytometry (ICFC), fixation with Fixation Buffer (Cat. No. 420801) followed by True-Phos™ Perm Buffer (Cat. No. 425401) is recommended.This antibody (clone W20235D) is not recommended for mouse or rat reactivity.

Host

Rat

Reactivity

Human

Application

WB - Quality testedIHC-P, ICC, ICFC - Verified

Platform ID

BAB522894621

BioLegend

Headquarters

8999 BioLegend Way San Diego, CA 92121 United States

Contact

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

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Product Specifications
Scientific Background

Specifications

NamePurified anti-TFAP2A Antibody, TFAP2A, W20235D
Cat. No.634351
HostRat
RRIDAB_3106151 (BioLegend Cat. No. 634351)AB_3106151 (BioLegend Cat. No. 634352)
IsotypeRat IgG2a, κ
ReactivityHuman
ApplicationWB - Quality testedIHC-P, ICC, ICFC - Verified
ClonalityMonoclonal
Clone NumberW20235D
Concentration0.5 mg/mL
TargetTFAP2A
ImmunogenRecombinant fragment of human TFAP2A
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

TFAP2A, or transcription factor AP-2-alpha, binds to a GC-rich DNA consensus sequence 5'-GCCNNNGGC-3'. Its functions are integral to numerous biological processes including embryonic ectodermal development, stem cell differentiation, and the regulation of cell growth and proliferation. TFAP2A is active in the neural crest and regulates a group of cells in the early embryo that give rise to many tissues and organs, including bones and other tissues of the head and neck. In humans, TFAP2A mutation causes Branchio-oculo-facial syndrome (BOFS). In kidney development, TFAP2A functions in distal nephron development dictating the progression of cells towards a fully differentiated state. TFAP2A is also involved in carcinogenesis and is highly expressed in various types of cancer, including bladder cancer, melanoma, head and neck squamous carcinoma, gastric cancer, ovarian cancer, lung adenocarcinoma, and nasopharyngeal carcinoma. In addition to its role in cancer, TFAP2A is a well-known regulator of craniofacial development and evolution.

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