TFAP2B antibody (C-Term)

Catalog No. ABIN657180

The Rabbit Polyclonal anti-TFAP2B antibody (Clone RB33155) (ABIN657180) specifically detects TFAP2B in WB. The antibody is reactive with Human samples.

Quick Overview for TFAP2B antibody (C-Term) (ABIN657180)

Target: TFAP2B (Transcription Factor AP-2 beta (Activating Enhancer Binding Protein 2 Beta) (TFAP2B))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This TFAP2B antibody is un-conjugated

Application: Western Blotting (WB)

Clone: RB33155

Product Details anti-TFAP2B Antibody

Binding Specificity: AA 431-462, C-Term

Predicted Reactivity: M

Purification: This antibody is purified through a protein A column, followed by peptide affinity purification.

Immunogen: This TFAP2B antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 431-462 amino acids from the C-terminal region of human TFAP2B.

Isotype: Ig Fraction

Application Details

Application Notes: WB: 1:1000

Restrictions: For Research Use only

Handling

Format: Liquid

Buffer: Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.

Preservative: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Expiry Date: 6 months

Target Details for TFAP2B

Target: TFAP2B (Transcription Factor AP-2 beta (Activating Enhancer Binding Protein 2 Beta) (TFAP2B))

Alternative Name: TFAP2B

Background: This gene encodes a member of the AP-2 family of transcription factors. AP-2 proteins form homo- or hetero-dimers with other AP-2 family members and bind specific DNA sequences. They are thought to stimulate cell proliferation and suppress terminal differentiation of specific cell types during embryonic development. Specific AP-2 family members differ in their expression patterns and binding affinity for different promoters. This protein functions as both a transcriptional activator and repressor. Mutations in this gene result in autosomal dominant Char syndrome, suggesting that this gene functions in the differentiation of neural crest cell derivatives. [provided by RefSeq].

Molecular Weight: 50474

NCBI Accession: NP_003212

UniProt: Q92481

Pathways: Carbohydrate Homeostasis, Synaptic Membrane