Western blot analysis of anti-TFAP2A Antibody (N-term) in NCI-H460 cell line lysates (35ug/lane). TFAP2A (arrow) was detected using the purified Pab (1:60 dilution).
TFAP2A; AP2TF; TFAP2; Transcription factor AP-2-alpha; AP-2 transcription factor; Activating enhancer-binding protein 2-alpha; Activator protein 2
Key Feature
Clonality
Polyclonal
Isotype
Ig
Host Species
Rabbit
Tested Applications
WB
WB:1:50~100
Species Reactivity
Human
Concentration
1mg/ml
Target Information
Gene Synonyms
AP2TF TFAP2
Alternative Names
TFAP2A AP2TF TFAP2 Transcription factor AP-2-alpha AP-2 transcription factor Activating enhancer-binding protein 2-alpha Activator protein 2
Molecular Weight(MW)
48062 Da
Function
Sequence-specific DNA-binding protein that interacts with inducible viral and cellular enhancer elements to regulate transcription of selected genes. AP-2 factors bind to the consensus sequence 5'-GCCNNNGGC-3' and activate genes involved in a large spectrum of important biological functions including proper eye, face, body wall, limb and neural tube development They also suppress a number of genes including MCAM/MUC18, C/EBP alpha and MYC. AP-2-alpha is the only AP-2 protein required for early morphogenesis of the lens vesicle. Together with the CITED2 coactivator, stimulates the PITX2 P1 promoter transcription activation. Associates with chromatin to the PITX2 P1 promoter region
Tissue Specificity
This TFAP2A antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide selected from the N-terminal region of human TFAP2A.
Western blot analysis of anti-TFAP2A Antibody (N-term) in NCI-H460 cell line lysates (35ug/lane). TFAP2A (arrow) was detected using the purified Pab (1:60 dilution).
Application Notes
WB:1:50~100
Additional Information
Form
Liquid
Storage Instructions
For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
Storage Buffer
Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS.