C9orf16 antibody (AA 1-83) (Biotin)

Catalog No. ABIN1701103

Product Details anti-C9orf16 Antibody (Biotin)

Target: C9orf16 (Chromosome 9 Open Reading Frame 16 (C9orf16))

Binding Specificity: AA 1-83

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C9orf16 antibody is conjugated to Biotin

Application: ELISA, Western Blotting (WB), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

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

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C9orf16

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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 for 12 months.

Expiry Date: 12 months

Target Details for C9orf16

Target: C9orf16 (Chromosome 9 Open Reading Frame 16 (C9orf16))

Alternative Name: C9orf16 (C9orf16 Products)

Synonyms: EST00098 antibody, chromosome 9 open reading frame 16 antibody, C9orf16 antibody

Background:

Synonyms: C9orf16, Chromosome 9 open reading frame 16, CI016_HUMAN, EST00098, FLJ12823, MGC4639, UPF0184 protein C9orf16.

Background: C9orf16 (chromosome 9 open reading frame 16) is an 83 amino acid protein that belongs to the UPF0184 (EST00098) family and is encoded by a gene that maps to human chromosome 9q34.11. 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: 79095