C1orf122 antibody (AA 11-80) (Biotin)

Catalog No. ABIN1699877

The Rabbit Polyclonal anti-C1orf122 antibody has been validated for WB, ELISA, IHC (fro) and IHC (p). It is suitable to detect C1orf122 in samples from Human.

Quick Overview for C1orf122 antibody (AA 11-80) (Biotin) (ABIN1699877)

Target: C1orf122 (Chromosome 1 Open Reading Frame 122 (C1orf122))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C1orf122 antibody is conjugated to Biotin

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

Product Details anti-C1orf122 Antibody (Biotin)

Binding Specificity: AA 11-80

Predicted Reactivity: Human,Rabbit

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C1orf122

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 C1orf122

Target: C1orf122 (Chromosome 1 Open Reading Frame 122 (C1orf122))

Alternative Name: C1orf122

Background:

Synonyms: ALAESM, Chromosome 1 open reading frame 122, FLJ23476, FLJ45459, Hypothetical protein LOC127687, Protein ALAESM, Uncharacterized protein C1orf122,CA122_HUMAN.

Background: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf122 gene product has been provisionally designated C1orf122 pending further characterization.

Gene ID: 127687