PRMT7 Antikörper (AA 513-692)

Produktnummer ABIN6146234

Der Kaninchen Polyklonal Anti-PRMT7-Antikörper wurde für WB validiert. Er ist geeignet, PRMT7 in Proben von Human zu detektieren.

Kurzübersicht für PRMT7 Antikörper (AA 513-692) (ABIN6146234)

Target: PRMT7 (Protein Arginine Methyltransferase 7 (PRMT7))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser PRMT7 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-PRMT7 Antikörper

Bindungsspezifität: AA 513-692

Sequenz: QAASLHAVVV EFRDLWRIRS PCGDCEGFDV HIMDDMIKRA LDFRESREAE PHPLWEYPCR SLSEPWQILT FDFQQPVPLQ PLCAEGTVEL RRPGQSHAAV LWMEYHLTPE CTLSTGLLEP ADPEGGCCWN PHCKQAVYFF SPAPDPRALL GGPRTVSYAV EFHPDTGDII MEFRHADTPD

Kreuzreaktivität: Human, Maus, Ratte

Produktmerkmale: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 513-692 of human PRMT7 (NP_061896.1).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:500 - 1:2000

Kommentare:

HIGH QUALITY

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 PRMT7

Target: PRMT7 (Protein Arginine Methyltransferase 7 (PRMT7))

Andere Bezeichnung: PRMT7

Hintergrund: This gene encodes a member of the protein arginine N-methyltransferase family of proteins. The encoded enzyme transfers single methyl groups to arginine residues to generate monomethylarginines on histone proteins as well as other protein substrates. This enzyme plays a role in a wide range of biological processes, including neuronal differentiation, male germ line imprinting, small nuclear ribonucleoprotein biogenesis, and regulation of the Wnt signaling pathway. Mutations in this gene underlie multiple related syndromes in human patients characterized by intellectual disability, short stature and other features. The encoded protein may promote breast cancer cell invasion and metastasis in human patients.,PRMT7,SBIDDS,Epigenetics & Nuclear Signaling,PRMT7

Molekulargewicht: 62 kDa/63 kDa/73 kDa/78 kDa

Gen-ID: 54496

UniProt: Q9NVM4

Pathways: Ribonucleoprotein Complex Subunit Organization