- Research Products Primary Antibodies: Mammalian Phospho-Specific Antibodies Antibodies for IHC (Paraffin) Staining Flow Cytometry Veterinary Research Antibodies Primary Antibodies: Non-Mammalian siRNA and shRNA (plasmid and lentivirus) Products Protein A, G PLUS and L-Agarose Tissue Extracts and Cell Lysates Biologically Active and Purified Proteins Transfected Cell Lysates Secondary Antibodies, Control Antibodies and Normal Sera Specialty Reagents and Kits
- Chemicals
- Lab Supplies
- Animal Health
- What's New
- Information
- Support
Welcome to Santa Cruz Biotechnology!
 | ||
| ||
KIAA0913 AntibodiesSanta Cruz Biotechnology, Inc. offers a broad range of KIAA0913 antibodies. Select KIAA0913 antibodies from several monoclonal and/or polyclonal KIAA0913 antibodies listed below. View detailed KIAA0913 antibody specifications by linking to the specific product blocks. Select appropriate KIAA0913 antibodies for your research by isotype, epitope, applications and species reactivity. KIAA0913 gene silencer products in siRNA, shRNA Plasmid and shRNA Lentiviral Particle formats are also available. Introducing HOVERcruz™,a unique system for rapid identification of KIAA0913 Antibodies. Hover over product names in the table to see representative data for each product.Live chat is now available! (click here)Our live chat system is available to answer your product and ordering questions.KIAA0913 is a 1,837 amino acid protein that contains one SWIM-type zinc finger and is post-translationally phosphorylated at serine residues 567, 1040 and 1042. KIAA0913 exists as five alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 10. Chromosome 10 contains over 800 genes and 135 million nucleotides, which makes up nearly 4.5% of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome, which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious. |