TSACC/C1orf182 antibody (AA 21-100) (Biotin)

Catalog No. ABIN1699884

Product Details anti-TSACC/C1orf182 Antibody (Biotin)

Target: TSACC/C1orf182 (TSACC) (TSSK6 Activating Co-Chaperone (TSACC))

Binding Specificity: AA 21-100

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This TSACC/C1orf182 antibody is conjugated to Biotin

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

Predicted Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C1orf182

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 TSACC/C1orf182

Target: TSACC/C1orf182 (TSACC) (TSSK6 Activating Co-Chaperone (TSACC))

Alternative Name: C1orf182 (TSACC Products)

Synonyms: SIP antibody, TP53DINP1 antibody, TP53INP1A antibody, TP53INP1B antibody, Teap antibody, p53DINP1 antibody, C1orf182 antibody, RP11-443G18.5 antibody, SSTK-IP antibody, 1700021C14Rik antibody, C3H1orf182 antibody, RGD1304953 antibody, tumor protein p53 inducible nuclear protein 1 antibody, TSSK6 activating cochaperone antibody, TSSK6 activating co-chaperone antibody, TP53INP1 antibody, TSACC antibody, Tsacc antibody

Background:

Synonyms: C1orf182, CA182_HUMAN, SSTK-interacting protein, SSTK-IP, Uncharacterized protein C1orf182.

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 C1orf182 gene product has been provisionally designated C1orf182 pending further characterization.

Gene ID: 128229