GTF2I antibody (C-Term)

Catalog No. ABIN453078

This anti-GTF2I antibody is a Rabbit Polyclonal antibody detecting GTF2I in WB and EIA. Suitable for Human.

Quick Overview for GTF2I antibody (C-Term) (ABIN453078)

Target: GTF2I (General Transcription Factor III (GTF2I))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This GTF2I antibody is un-conjugated

Application: Western Blotting (WB), Enzyme Immunoassay (EIA)

Product Details anti-GTF2I Antibody

Binding Specificity: C-Term

Specificity: This antibody detects GTF2I / TFII-I at C-term.

Cross-Reactivity (Details): Species reactivity (tested):Human

Purification: Purified through a protein A column, followed by peptide affinity purification

Immunogen: KLH conjugated synthetic peptide selected from the C-terminal region of human GTF2I

Application Details

Application Notes: Western blot: 1: 100 - 1: 500. ELISA: 1: 1,000.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user.

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 0.25 mg/mL

Buffer: 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.

Handling Advice: Avoid repeated freezing and thawing.

Storage: 4 °C/-20 °C

Storage Comment: Store the antibody at 2 - 8 °C up to one month or (in aliquots) at -20 °C for longer.

Target Details for GTF2I

Target: GTF2I (General Transcription Factor III (GTF2I))

Alternative Name: GTF2I / TFII-I

Background: GTF2I is a multifunctional phosphoprotein with roles in transcription and signal transduction. It is deleted in Williams-Beuren syndrome, a multisystem developmental disorder caused by the deletion of contiguous genes at chromosome 7q11.23.Synonyms: BAP-135, BAP135, Bruton tyrosine kinase-associated protein 135, GTFII-I, General transcription factor II-I, SPIN, SRF-Phox1-interacting protein, WBSCR6, Williams-Beuren syndrome chromosomal region 6 protein

Molecular Weight: 112416 Da

Gene ID: 2969

NCBI Accession: NP_001509

UniProt: P78347