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Thermo Fisher Scientific WRN Polyclonal Antibody
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Thermo Fisher Scientific WRN Polyclonal Antibody

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Human WRN 단백질을 인식하는 Rabbit Polyclonal Antibody로, IHC(P) 및 ICC/IF에 사용 가능. 항원 친화 크로마토그래피로 정제되었으며, PBS와 글리세롤 버퍼에 보관. 4°C 단기, -20°C 장기 보관 권장. 연구용으로만 사용.

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pk
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마지막 업데이트 2025. 08. 05. 오전 05:36
Thermo Fisher Scientific PA583025 WRN Polyclonal Antibody 100 ul pk판매 단위 pk ·
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740,000원VAT 포함 814,000원

Thermo Fisher Scientific · Thermo Fisher Scientific WRN Polyclonal Antibody

Applications

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: 1:50–1:200

Immunocytochemistry (ICC/IF)

  • Tested Dilution: 0.25–2 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human WRN. Recombinant protein control fragment (Product # RP-89491)
Conjugate Unconjugated
Form Liquid
Concentration 0.1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 40% glycerol
Contains 0.02% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2790181

Product Specific Information

Immunogen sequence:
KADIRQVIHY GAPKDMESYY QEIGRAGRDG LQSSCHVLWA PADINLNRHL LTEIRNEKFR LYKLKMMAKM EKYLHSSRCR RQIILSHFED KQVQKASLGI MGTEKCCDNC RSRLDHCYSM DDSEDTSWDF GPQAFKLLSA VD


Target Information

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.


For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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