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APM2 Antibodies

Santa Cruz Biotechnology, Inc. offers a broad range of APM2 antibodies. Select APM2 antibodies from several monoclonal and/or polyclonal APM2 antibodies listed below. View detailed APM2 antibody specifications by linking to the specific product blocks. Select appropriate APM2 antibodies for your research by isotype, epitope, applications and species reactivity. APM2 gene silencer products in siRNA, shRNA Plasmid and shRNA Lentiviral Particle formats are also available.

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a unique system for rapid identification of APM2 Antibodies. Hover over product names in the table to see representative data for each product.

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PRODUCT NAMECAT. #ISOTYPEEPITOPEAPPLICATIONSSPECIESCITATIONSRATING
APM2 (C-14)sc-139452rabbit IgGC-terminal (h)WB, IF, ELISAhuman
APM2 (N-15)sc-139450rabbit IgGN-terminal (h)WB, IF, ELISAhuman

APM2 siRNA, shRNA Plasmid and shRNA Lentiviral Particles gene silencers include:

siRNAsshRNA PlasmidsshRNA Lentiviral ParticlesCITATIONSRANKING
APM2 siRNA (h): sc-90461APM2 shRNA Plasmid (h):
sc-90461-SH
APM2 shRNA (h)
Lentiviral Particles: sc-90461-V

APM2 (adipose most abundant gene transcript 2), also known as C10orf116, is a 76 amino acid protein that is expressed in liver, cornea and adipose tissue and is encoded by a gene which maps to human chromosome 10. Chromosome 10 houses over 1,200 genes and comprises nearly 4.5% of the human genome. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman’s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.