C9orf78 antibody (AA 21-120)

Catalog No. ABIN1714707

This anti-C9orf78 antibody is a Rabbit Polyclonal antibody detecting C9orf78 in WB, IF (cc), IF (p), ELISA, IHC (p), ICC and IHC (fro). Suitable for Human.

Quick Overview for C9orf78 antibody (AA 21-120) (ABIN1714707)

Target: C9orf78 (C9orf98) (Chromosome 9 Open Reading Frame 78 (C9orf98))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C9orf78 antibody is un-conjugated

Application: Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC), Immunohistochemistry (Frozen Sections) (IHC (fro))

Product Details anti-C9orf78 Antibody

Binding Specificity: AA 21-120

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

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C9orf78

Isotype: IgG

Application Details

Application Notes: WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500

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 C9orf78

Target: C9orf78 (C9orf98) (Chromosome 9 Open Reading Frame 78 (C9orf98))

Alternative Name: C9orf78

Background:

Synonyms: bA409K20.3, C9orf78, Chromosome 9 open reading frame 78, CI078_HUMAN, HCA59, Hepatocellular carcinoma associated antigen 59, Hepatocellular carcinoma-associated antigen 59, HSPC220, Uncharacterized protein C9orf78.

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 C9orf78 gene product has been provisionally designated C9orf78 pending further characterization.

Gene ID: 51759