RECQL2 Antikörper (AA 1223-1432)

Produktnummer ABIN6150263

Dieses Anti-RECQL2-Antikörper ist ein Kaninchen Polyklonal-Antikörper zur Detektion von RECQL2 in WB. Geeignet für Human.

Kurzübersicht für RECQL2 Antikörper (AA 1223-1432) (ABIN6150263)

Target: RECQL2 (WRN) (Werner syndrome RecQ like helicase (WRN))

Reaktivität: Human

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser RECQL2 Antikörper ist unkonjugiert

Applikation: Western Blotting (WB)

Produktdetails anti-RECQL2 Antikörper

Bindungsspezifität: AA 1223-1432

Sequenz: CQTNSVQTDL FSSTKPQEEQ KTSLVAKNKI CTLSQSMAIT YSLFQEKKMP LKSIAESRIL PLMTIGMHLS QAVKAGCPLD LERAGLTPEV QKIIADVIRN PPVNSDMSKI SLIRMLVPEN IDTYLIHMAI EILKHGPDSG LQPSCDVNKR RCFPGSEEIC SSSKRSKEEV GINTETSSAE RKRRLPVWFA KGSDTSKKLM DKTKRGGLFS

Kreuzreaktivität: Human

Produktmerkmale: Polyclonal Antibodies

Immunogen: Recombinant fusion protein containing a sequence corresponding to amino acids 1223-1432 of human WRN (NP_000544.2).

Isotyp: IgG

Anwendungsinformationen

Applikationshinweise: WB,1:200 - 1:1000

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 RECQL2

Target: RECQL2 (WRN) (Werner syndrome RecQ like helicase (WRN))

Andere Bezeichnung: WRN

Hintergrund: This gene encodes a member of the RecQ subfamily and the DEAH (Asp-Glu-Ala-His) subfamily of DNA and RNA helicases. DNA helicases are involved in many aspects of DNA metabolism, including transcription, replication, recombination, and repair. This protein contains a nuclear localization signal in the C-terminus and shows a predominant nucleolar localization. It possesses an intrinsic 3' to 5' DNA helicase activity, and is also a 3' to 5' exonuclease. Based on interactions between this protein and Ku70/80 heterodimer in DNA end processing, this protein may be involved in the repair of double strand DNA breaks. Defects in this gene are the cause of Werner syndrome, an autosomal recessive disorder characterized by premature aging.,WRN,RECQ3,RECQL2,RECQL3,Epigenetics & Nuclear Signaling,DNA Damage & Repair,Cell Biology & Developmental Biology,Apoptosis,WRN

Molekulargewicht: 162 kDa

Gen-ID: 7486

UniProt: Q14191

Pathways: DNA Reparatur