C16orf57 Antikörper (AA 1-265)

Produktnummer ABIN6149979

Produktdetails anti-C16orf57 Antikörper

Target: C16orf57 (USB1) (U6 SnRNA Biogenesis 1 (USB1))

Bindungsspezifität: AA 1-265

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser C16orf57 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Sequenz: MSAAPLVGYS SSGSEDESED GMRTRPGDGS HRRGQSPLPR QRFPVPDSVL NMFPGTEEGP EDDSTKHGGR VRTFPHERGN WATHVYVPYE AKEEFLDLLD VLLPHAQTYV PRLVRMKVFH LSLSQSVVLR HHWILPFVQA LKARMTSFHR FFFTANQVKI YTNQEKTRTF IGLEVTSGHA QFLDLVSEVD RVMEEFNLTT FYQDPSFHLS LAWCVGDARL QLEGQCLQEL QAIVDGFEDA EVLLRVHTEQ VRCKSGNKFF SMPLK

Kreuzreaktivität: Human, Maus

Produktmerkmale: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1-265 of human USB1 (NP_078874.2).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Buffer: PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.

Konservierungsmittel: Sodium azide

Vorsichtsmaßnahmen: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Lagerung: -20 °C

Informationen zur Lagerung: Store at -20°C. Avoid freeze / thaw cycles.

Details zu C16orf57

Target: C16orf57 (USB1) (U6 SnRNA Biogenesis 1 (USB1))

Andere Bezeichnung: USB1 (USB1 Produkte)

Synonyme: C16orf57 antikoerper, HVSL1 antikoerper, Mpn1 antikoerper, PN antikoerper, hUsb1 antikoerper, C18H16orf57 antikoerper, AA960436 antikoerper, RGD1305215 antikoerper, c16orf57 antikoerper, C2H16orf57 antikoerper, zgc:91896 antikoerper, U6 snRNA biogenesis phosphodiesterase 1 antikoerper, U6 snRNA biogenesis 1 antikoerper, U6 snRNA biogenesis phosphodiesterase 1 L homeolog antikoerper, USB1 antikoerper, Usb1 antikoerper, usb1.L antikoerper, usb1 antikoerper

Hintergrund: This gene encodes a protein with several conserved domains, however, its exact function is not known. Mutations in this gene are associated with poikiloderma with neutropenia (PN), which shows phenotypic overlap with Rothmund-Thomson syndrome (RTS) caused by mutations in the RECQL4 gene. It is believed that this gene product interacts with RECQL4 protein via SMAD4 proteins, explaining the partial clinical overlap between PN and RTS. Alternatively spliced transcript variants encoding different isoforms have been noted for this gene.,USB1,C16orf57,HVSL1,Mpn1,PN,hUsb1,Cell Biology & Developmental Biology,USB1

Molekulargewicht: 20 kDa/28 kDa/30 kDa

Gen-ID: 79650

UniProt: Q9BQ65