C9orf68 antibody (AA 201-300) (Cy5)

Catalog No. ABIN1703576

The Rabbit Polyclonal anti-C9orf68 antibody has been validated for IF (cc) and IF (p). It is suitable to detect C9orf68 in samples from Human.

Quick Overview for C9orf68 antibody (AA 201-300) (Cy5) (ABIN1703576)

Target: C9orf68 (Chromosome 9 Open Reading Frame 68 (C9orf68))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C9orf68 antibody is conjugated to Cy5

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

Product Details anti-C9orf68 Antibody (Cy5)

Binding Specificity: AA 201-300

Predicted Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C9orf68

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 C9orf68

Target: C9orf68 (Chromosome 9 Open Reading Frame 68 (C9orf68))

Alternative Name: C9orf68

Background:

Synonyms: bA6J24.2, chromosome 9 open reading frame 68, FLJ10058, RP11-280I16.2, Uncharacterized protein C9orf68,SPA6L_HUMAN.

Background: Chromosome 9 consists of about 145 million bases and 4 % of the human genome and encodes nearly 900 genes. Considered 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. The C9orf68 gene product has been provisionally designated C9orf68 pending further characterization. There are two isoforms of C9orf68 that are produced as a result of alternative splicing events.

Gene ID: 55064