CLUAP1 antibody (AA 35-140) (Cy7)

Catalog No. ABIN721111

This Rabbit Polyclonal antibody specifically detects CLUAP1 in WB, IF (cc) and IF (p). It exhibits reactivity toward Human.

Quick Overview for CLUAP1 antibody (AA 35-140) (Cy7) (ABIN721111)

Target: CLUAP1 (Clusterin Associated Protein 1 (CLUAP1))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This CLUAP1 antibody is conjugated to Cy7

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-CLUAP1 Antibody (Cy7)

Binding Specificity: AA 35-140

Predicted Reactivity: Human,Mouse,Rat,Dog,Sheep,Pig,Horse,Chicken,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human CLUAP1

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Preservative: ProClin

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

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for CLUAP1

Target: CLUAP1 (Clusterin Associated Protein 1 (CLUAP1))

Alternative Name: CLUAP1

Background:

Synonyms: Clusterin associated protein 1, FLJ13297, KIAA0643, CLUA1_HUMAN.

Background: CLUAP1 (Clusterin associated protein 1) is a 413 amino acid nuclear protein that exists as two alternatively spliced isoforms that interact with Clusterin. CLUAP1 is suggested to play a role in apoptosis and cell proliferation, and is expressed in testis, thrachea and thyroid, with low levels found in adrenal gland and spinal cord. The gene encoding CLUAP1 maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3 % of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, which is a gastrointestinal inflammatory condition.

Gene ID: 23059