AHI1 antibody (N-Term)

Catalog No. ABIN2854592

The Rabbit Polyclonal anti-AHI1 antibody has been validated for WB. It is suitable to detect AHI1 in samples from Human.

Quick Overview for AHI1 antibody (N-Term) (ABIN2854592)

Target: AHI1 (Abelson Helper Integration Site 1 (AHI1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This AHI1 antibody is un-conjugated

Application: Western Blotting (WB)

Product Details anti-AHI1 Antibody

Binding Specificity: N-Term

Cross-Reactivity: Human

Characteristics: Rabbit Polyclonal antibody to AHI1 (Abelson helper integration site 1)
AHI1 antibody [N1], N-term

Purification: Purified by antigen-affinity chromatography.

Immunogen: Carrier-protein conjugated synthetic peptide encompassing a sequence within the N-terminus region of human AHI1. The exact sequence is proprietary.

Isotype: IgG

Application Details

Application Notes: WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

Comment:

Positive Control: NT2D1

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 mg/mL

Buffer: 0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

Preservative: Thimerosal (Merthiolate)

Precaution of Use: This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: 4 °C,-20 °C

Storage Comment: Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.

Target Details for AHI1

Target: AHI1 (Abelson Helper Integration Site 1 (AHI1))

Alternative Name: Abelson helper integration site 1

Background: This gene is apparently required for both cerebellar and cortical development in humans. This gene mutations cause specific forms of Joubert syndrome-related disorders. Joubert syndrome (JS) is a recessively inherited developmental brain disorder with several identified causative chromosomal loci. Alternatively spliced transcript variants encoding different isoforms have been identified.

Molecular Weight: 137 kDa

Gene ID: 54806

UniProt: Q8N157