CDNA Sequence BC051142 (BC051142) antibody (Biotin)

Catalog No. ABIN1403263

Product Details

Target: CDNA Sequence BC051142 (BC051142)

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: Biotin

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

Cross-Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human TSBP

Isotype: IgG

Application Details

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

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

Target: CDNA Sequence BC051142 (BC051142)

Alternative Name: TSBP (BC051142 Products)

Synonyms: SH2BP1 antibody, TSBP antibody, p150 antibody, p150TSP antibody, NG8 antibody, Tesb antibody, Tesbp antibody, CTR9 homolog, Paf1/RNA polymerase II complex component antibody, chromosome 6 open reading frame 10 antibody, cDNA sequence BC051142 antibody, testis specific basic protein antibody, CTR9 antibody, C6orf10 antibody, BC051142 antibody, Tesb antibody

Background:

Synonyms: C6orf10, CF010_HUMAN, Chromosome 6 open reading frame 10, Testis specic basic protein, TSBP, Uncharacterized protein C6orf10.

Background: 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 C6orf10 gene product has been provisionally designated C6orf10 pending further characterization.

Gene ID: 9646

Pathways: Cellular Response to Molecule of Bacterial Origin, Stem Cell Maintenance