C6orf129 antibody (AA 1-50) (Biotin)

Catalog No. ABIN1701477

Product Details anti-C6orf129 Antibody (Biotin)

Target: C6orf129 (CCDC167) (Coiled-Coil Domain Containing 167 (CCDC167))

Binding Specificity: AA 1-50

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C6orf129 antibody is conjugated to Biotin

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

Predicted Reactivity: Human,Mouse,Rat,Cow,Sheep,Pig

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C6orf129

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 C6orf129

Target: C6orf129 (CCDC167) (Coiled-Coil Domain Containing 167 (CCDC167))

Alternative Name: C6orf129 (CCDC167 Products)

Synonyms: C6orf129 antibody, HSPC265 antibody, C23H6orf129 antibody, 1110021J02Rik antibody, coiled-coil domain containing 167 antibody, CCDC167 antibody, Ccdc167 antibody

Background:

Synonyms: CCDC167, C6orf129, CCDC167, CC167_HUMAN, Chromosome 6 open reading frame 129, Coiled coil domain containing 167, HSPC265, RP1-153P14.2, Transmembrane and coiled-coil domain-containing protein C6orf129.

Background: C6orf129 is a Making up nearly 6 % of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6. The C6orf129 gene product has been provisionally designated C6orf129 pending further characterization.

Gene ID: 154467