Produktinformation Diagnostik & molekulare Diagnostik Laborgeräte & Service Zellkultur & Verbrauchsmaterial Forschungsprodukte & Biochemikalien Weitere Information auf den folgenden Seiten! See the following pages for more information! Lieferung & Zahlungsart Lieferung: frei Haus Bestellung auf Rechnung SZABO-SCANDIC Lieferung: € 10,- HandelsgmbH & Co KG Erstbestellung Vorauskassa Quellenstraße 110, A-1100 Wien T. +43(0)1 489 3961-0 Zuschläge F. +43(0)1 489 3961-7 [email protected] • Mindermengenzuschlag www.szabo-scandic.com • Trockeneiszuschlag • Gefahrgutzuschlag linkedin.com/company/szaboscandic • Expressversand facebook.com/szaboscandic Tel:240-252-7368(USA) Fax:240-252-7376(USA) www.elabscience.com ® E-mail:[email protected] Elabscience Elabscience Biotechnology Inc. FAM107B Polyclonal Antibody Catalog No. E-AB-53033 Reactivity H,M,R Storage Store at -20℃. Avoid freeze / thaw cycles. Host Rabbit Applications IHC,ELISA Isotype IgG Note: Centrifuge before opening to ensure complete recovery of vial contents. Images Immunogen Information Immunogen Fusion protein of human FAM107B Gene Accession BC004872 Swissprot Q9H098 Synonyms C10orf45,F107B,FAM107B,Family with sequence similarity 107, member B,FLJ45505,MGC11034,Protein FAM107B Immunohistochemistry of paraffin- Product Information embedded Human tonsil tissue using Buffer PBS with 0.05% NaN3 and 40% Glycerol,pH7.4 FAM107B Polyclonal Antibody at Purify Antigen affinity purification dilution of 1:160(×200) Dilution IHC 1:150-1:300, ELISA 1:5000-1:10000 Background FAM107B is a 131 amino acid protein that is encoded by a gene that maps to human chromosome 10, which contains over 800 genes and 135 Immunohistochemistry of paraffin- million nucleotides, making up nearly 4.5% of the human genome. PTEN embedded Human brain tissue using is an important tumor suppressor gene located on chromosome 10 and, FAM107B Polyclonal Antibody at when defective, causes a genetic predisposition to cancer development dilution of 1:160(×200) 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. For Research Use Only Focus on your research Thank you for your recent purchase. If you would like to learn more about antibodies,please visit www.elabscience.com. Service for life science Applications:WB-Western Blot IHC-Immunohistochemistry IF-Immunofluorescence IP-Immunoprecipitation FC-Flow cytometry ChIP- Chromatin Immunoprecipitation Reactivity: H-Human R-Rat M-Mouse Mk-Monkey Dg-Dog Ch-Chicken Hm-Hamster Rb-Rabbit Sh- Sheep Pg-Pig Z-Zebrafish X-Xenopus C-Cow. Powered by TCPDF (www.tcpdf.org).