C8orf12 antibody (AA 1-80) (Cy7)

Catalog No. ABIN1707329

The Rabbit Polyclonal anti-C8orf12 antibody has been validated for IF (cc) and IF (p). It is suitable to detect C8orf12 in samples from Human.

Quick Overview for C8orf12 antibody (AA 1-80) (Cy7) (ABIN1707329)

Target: C8orf12 (C8ORF12) (Chromosome 8 Open Reading Frame 12 (C8ORF12))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C8orf12 antibody is conjugated to Cy7

Application: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-C8orf12 Antibody (Cy7)

Binding Specificity: AA 1-80

Cross-Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C8orf12

Isotype: IgG

Application Details

Application Notes: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 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: 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Expiry Date: 12 months

Target Details for C8orf12

Target: C8orf12 (C8ORF12) (Chromosome 8 Open Reading Frame 12 (C8ORF12))

Alternative Name: C8orf12

Background:

Synonyms: Chromosome 8 open reading frame 12, Uncharacterized protein C8orf12, CH012_HUMAN.

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 C8orf12 gene product has been provisionally designated C8orf12 pending further characterization.