TFAP2A Antilichaam

The protein encoded by this gene is a transcription factor that binds the consensus sequence 5'-GCCNNNGGC-3'. The encoded protein functions as either a homodimer or as a heterodimer with similar family members. This protein activates the transcription of some genes while inhibiting the transcription of others. Defects in this gene are a cause of branchiooculofacial syndrome (BOFS) . Three transcript variants encoding different isoforms have been found for this gene.

7020

P05549

Human, Mouse

Recombinant fusion protein containing a sequence corresponding to amino acids 1-437 of human TFAP2A (NP_001027451.1) .

Unconjugated

Primary Antibodies

Transcription

Affinity purification

Mouse eye

Batch dependent

PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

None

Blue Ice

Store at -20˚ C. Avoid freeze / thaw cycles.

Observed: 50kDa

IgG

TFAP2A

Transcription factor AP-2 alpha (activating enhancer binding protein 2 alpha)

Homo sapiens

TFAP2A, AP-2, BOFS, AP2TF, TFAP2, AP-2alpha

WB, IHC

Liquid