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FAM135 Antibodies

Santa Cruz Biotechnology, Inc. offers a broad range of FAM135 antibodies. Select FAM135 antibodies from several monoclonal and/or polyclonal FAM135 antibodies listed below. View detailed FAM135 antibody specifications by linking to the specific product blocks. Select appropriate FAM135 antibodies for your research by isotype, epitope, applications and species reactivity. FAM135 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 FAM135 Antibodies. Hover over product names in the table to see representative data for each product.

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Also see additional FAM135 Antibodies including, FAM135A, FAM135B

PRODUCT NAMECAT. #ISOTYPEEPITOPEAPPLICATIONSSPECIESCITATIONSRATING
FAM135B (K-16)sc-87719rabbit IgGInternal (h)WB, IF, ELISAm, r, h, e, c, p
FAM135B (N-13)sc-87720rabbit IgGN-terminus (h)WB, IF, ELISAm, h > r

FAM135 siRNA, shRNA Plasmid and shRNA Lentiviral Particles gene silencers include:

siRNAsshRNA PlasmidsshRNA Lentiviral ParticlesCITATIONSRANKING
FAM135A siRNA (h): sc-95221FAM135A shRNA Plasmid (h):
sc-95221-SH
FAM135A shRNA (h)
Lentiviral Particles: sc-95221-V
FAM135B siRNA (h): sc-77578FAM135B shRNA Plasmid (h):
sc-77578-SH
FAM135B shRNA (h)
Lentiviral Particles: sc-77578-V

Made up of nearly 146 million bases, chromosome 8 encodes about 800 genes. Translocation of portions of chromosome 8 with amplifications of the c-Myc gene are found in some leukemias and lymphomas, and typically associated with a poor prognosis. Portions of chromosome 8 have been linked to schizophrenia and bipolar disorder. Trisomy 8, also known as Warkany syndrome 2, most often results in early miscarriage but is occasionally seen in a mosaic form in surviving patients who suffer to a varying degree from a number of symptoms including retarded mental and motor development, and certain facial and developmental defects. WRN is a DNA helicase encoded by chromosome 8 and shown defective in those with the early aging disorder Werner syndrome. Chromosome 8 is also associated with Pfeiffer syndrome, congenital hypothyroidism and Waardenburg syndrome. The FAM135B gene product has been provisionally designated FAM135B pending further characterization.