C8orf47 antibody (FITC)

Catalog No. ABIN1709144

The Rabbit Polyclonal anti-C8orf47 antibody has been validated for WB. It is suitable to detect C8orf47 in samples from Human.

Quick Overview for C8orf47 antibody (FITC) (ABIN1709144)

Target: C8orf47 (C8ORF47) (Chromosome 8 Open Reading Frame 47 (C8ORF47))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C8orf47 antibody is conjugated to FITC

Application: Western Blotting (WB)

Product Details anti-C8orf47 Antibody (FITC)

Cross-Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C8orf47

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200

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.

Expiry Date: 12 months

Target Details for C8orf47

Target: C8orf47 (C8ORF47) (Chromosome 8 Open Reading Frame 47 (C8ORF47))

Alternative Name: C8orf47

Background:

Synonyms: C8orf47, CH047_HUMAN, Chromosome 8 open reading frame 47, Uncharacterized protein C8orf47.

Background: Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The C8orf47 gene product has been provisionally designated C8orf47 pending further characterization.

Gene ID: 203111