CDNA Sequence BC051142 (BC051142) antibody (PE)

Catalog No. ABIN2179829

The Rabbit Polyclonal anti- antibody has been validated for WB. It is suitable to detect in samples from Human.

Quick Overview for CDNA Sequence BC051142 (BC051142) antibody (PE) (ABIN2179829)

Target: CDNA Sequence BC051142 (BC051142)

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: PE

Application: Western Blotting (WB)

Product Details

Cross-Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human TSBP

Isotype: IgG

Application Details

Application Notes: FCM: (1:20-100)
Optimal working dilution should be determined by the investigator.

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: Sodium azide

Precaution of Use: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Storage: -20 °C

Storage Comment: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Target Details

Target: CDNA Sequence BC051142 (BC051142)

Alternative Name: TSBP

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