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FAM22 Antibodies

Santa Cruz Biotechnology, Inc. offers a broad range of FAM22 antibodies. Select FAM22 antibodies from several monoclonal and/or polyclonal FAM22 antibodies listed below. View detailed FAM22 antibody specifications by linking to the specific product blocks. Select appropriate FAM22 antibodies for your research by isotype, epitope, applications and species reactivity. FAM22 gene silencer products in siRNA, shRNA Plasmid and shRNA Lentiviral Particle formats are also available.

Introducing HOVERcruz™,

a unique system for rapid identification of FAM22 Antibodies. Hover over product names in the table to see representative data for each product.

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Our live chat system is available to answer your product and ordering questions.

Also see additional FAM22 Antibodies including, FAM22F, FAM22G

PRODUCT NAMECAT. #ISOTYPEEPITOPEAPPLICATIONSSPECIESCITATIONSRATING
FAM22F/G (S-15)sc-246683goat IgGC-terminus (h)WB, IF, ELISAhuman
FAM22A/B/C/E (N-16)sc-323831goat IgGN-terminal (h)WB, IF, ELISAhuman

FAM22 siRNA, shRNA Plasmid and shRNA Lentiviral Particles gene silencers include:

siRNAsshRNA PlasmidsshRNA Lentiviral ParticlesCITATIONSRANKING
FAM22G siRNA (h): sc-92779FAM22G shRNA Plasmid (h):
sc-92779-SH
FAM22G shRNA (h)
Lentiviral Particles: sc-92779-V

FAM22F and FAM22G are members of the FAM22 family and are both expressed as two alternatively spliced isoforms. The genes encoding FAM22F and FAM22G map to human chromosome 9, which consists of about 145 million bases and 4% of the human genome and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.