C3orf49 antibody (FITC)

Catalog No. ABIN1404926

The Rabbit Polyclonal anti-C3orf49 antibody is suitable to detect C3orf49 in samples from Human. It has been validated for IF.

Quick Overview for C3orf49 antibody (FITC) (ABIN1404926)

Target: C3orf49 (Chromosome 3 Open Reading Frame 49 (C3orf49))

Reactivity: Human

Host: Rabbit

Clonality: Polyclonal

Conjugate: This C3orf49 antibody is conjugated to FITC

Application: Immunofluorescence (IF)

Product Details anti-C3orf49 Antibody (FITC)

Purpose: C3orf49 Polyclonal Antibody, FITC Conjugated

Cross-Reactivity: Human

Purification: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human C3orf49

Isotype: IgG

Application Details

Application Notes: IF()

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, 0.02 % 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 C3orf49

Target: C3orf49 (Chromosome 3 Open Reading Frame 49 (C3orf49))

Alternative Name: C3orf49

Background:

Synonyms: chromosome 3 open reading frame 49, MGC17310, CC049_HUMAN.

Background: C3orf49 is a 292 amino acid protein encoded by a gene that maps to human chromosome 3p14.1. 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: 132200