C9ORF173 antibody (AA 201-300)

Catalog No. ABIN1714428

This anti-C9ORF173 antibody is a Rabbit Polyclonal antibody detecting C9ORF173 in WB and ELISA. Suitable for Mouse.

Quick Overview for C9ORF173 antibody (AA 201-300) (ABIN1714428)

Target: C9ORF173 (Chromosome 9 Open Reading Frame 173 (C9ORF173))

Reactivity: Mouse

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C9ORF173 antibody is un-conjugated

Application: Western Blotting (WB), ELISA

Product Details anti-C9ORF173 Antibody

Binding Specificity: AA 201-300

Cross-Reactivity: Mouse

Predicted Reactivity: Human,Rat,Dog

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C9orf173

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
ELISA 1:500-1000

Restrictions: For Research Use only

Handling

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Storage Comment: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Expiry Date: 12 months

Target Details for C9ORF173

Target: C9ORF173 (Chromosome 9 Open Reading Frame 173 (C9ORF173))

Alternative Name: C9orf173

Background:

Synonyms: C9orf173, Chromosome 9 open reading frame 173, CI173_HUMAN, Uncharacterized protein C9orf173.

Background: C9orf173 (chromosome 9 open reading frame 173) is a 389 amino acid protein that exists as four alternatively spliced isoforms. The gene encoding C9orf173 maps to human chromosome 9q34.3. Chromosome 9 consists of about 145 million bases, represents 4 % of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.

Gene ID: 441476