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FAM82 Antibodies

Santa Cruz Biotechnology, Inc. offers a broad range of FAM82 antibodies. Select FAM82 antibodies from several monoclonal and/or polyclonal FAM82 antibodies listed below. View detailed FAM82 antibody specifications by linking to the specific product blocks. Select appropriate FAM82 antibodies for your research by isotype, epitope, applications and species reactivity. FAM82 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 FAM82 Antibodies. Hover over product names in the table to see representative data for each product.

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Also see additional FAM82 Antibodies including, FAM82A, FAM82B

PRODUCT NAMECAT. #ISOTYPEEPITOPEAPPLICATIONSSPECIESCITATIONSRATING
FAM82A (G-14)sc-167825goat IgGInternal (h)WB, IF, ELISAm, r, h, c, b, p
FAM82A (Y-14)sc-167827goat IgGInternal (h)WB, IF, ELISAm, r, h, c, b

FAM82 siRNA, shRNA Plasmid and shRNA Lentiviral Particles gene silencers include:

siRNAsshRNA PlasmidsshRNA Lentiviral ParticlesCITATIONSRANKING
FAM82A siRNA (h): sc-94982FAM82A shRNA Plasmid (h):
sc-94982-SH
FAM82A shRNA (h)
Lentiviral Particles: sc-94982-V
FAM82A siRNA (m): sc-145056FAM82A shRNA Plasmid (m):
sc-145056-SH
FAM82A shRNA (m)
Lentiviral Particles: sc-145056-V
FAM82B siRNA (h): sc-77449FAM82B shRNA Plasmid (h):
sc-77449-SH
FAM82B shRNA (h)
Lentiviral Particles: sc-77449-V

The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8% of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alström syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes. The FAM82A gene product has been provisionally designated FAM82A pending further characterization.