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TMEM89 Antibodies

Santa Cruz Biotechnology, Inc. offers a broad range of TMEM89 antibodies. Select TMEM89 antibodies from several monoclonal and/or polyclonal TMEM89 antibodies listed below. View detailed TMEM89 antibody specifications by linking to the specific product blocks. Select appropriate TMEM89 antibodies for your research by isotype, epitope, applications and species reactivity. TMEM89 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 TMEM89 Antibodies. Hover over product names in the table to see representative data for each product.

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TMEM89 (G-15)sc-100199rabbit IgGExtracellular (h)WB, IF, ELISAhuman
TMEM89 (P-19)sc-100201rabbit IgGExtracellular (h)WB, IF, ELISAm, r, h, e, c, b, p

TMEM89 siRNA, shRNA Plasmid and shRNA Lentiviral Particles gene silencers include:

siRNAsshRNA PlasmidsshRNA Lentiviral ParticlesCITATIONSRANKING
TMEM89 siRNA (h): sc-78294TMEM89 shRNA Plasmid (h):
TMEM89 shRNA (h)
Lentiviral Particles: sc-78294-V
TMEM89 siRNA (m): sc-154509TMEM89 shRNA Plasmid (m):
TMEM89 shRNA (m)
Lentiviral Particles: sc-154509-V

TMEM89 (transmembrane protein 89) is a 159 amino acid multi-pass membrane protein that is encoded by a gene which maps to human chromosome 3. Chromosome 3 is made up of about 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.