C3orf18 antibody (Cy7)

Catalog No. ABIN1422758

The Rabbit Polyclonal anti-C3orf18 antibody has been validated for WB and IF (p). It is suitable to detect C3orf18 in samples from Human, Mouse and Rat.

Quick Overview for C3orf18 antibody (Cy7) (ABIN1422758)

Target: C3orf18 (Chromosome 3 Open Reading Frame 18 (C3orf18))

Reactivity: Human, Mouse, Rat

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C3orf18 antibody is conjugated to Cy7

Application: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Product Details anti-C3orf18 Antibody (Cy7)

Cross-Reactivity: Human, Mouse, Rat

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C3orf18

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: 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 C3orf18

Target: C3orf18 (Chromosome 3 Open Reading Frame 18 (C3orf18))

Alternative Name: C3orf18

Background:

Synonyms: C3orf18, CC018_HUMAN, Protein G20, chromosome 3 open reading frame 18, Uncharacterized protein C3orf18.

Background: C3orf18, also known as G20, is a 162 amino acid single pass membrane protein that is encoded by a gene mapping to human chromosome 3q25.3. Chromosome 3 is made up of approximately 214 million bases encoding over 1,100 genes. Notably, there is a chemokine receptor gene cluster and a variety of human cancer related loci on chromosome 3. Particular regions of the chromosome 3 short arm are deleted in many types of cancer cells. Key tumor suppressing genes on chromosome 3 encode apoptosis mediator RASSF1, cell migration regulator HYAL1 and angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth disease are a few of the numerous genetic diseases associated with chromosome 3.

Gene ID: 51161