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Thermo Fisher Scientific DKC1 Polyclonal Antibody
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Thermo Fisher Scientific DKC1 Polyclonal Antibody

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Thermo Fisher Scientific DKC1 Polyclonal Antibody는 인간 DKC1 단백질을 인식하는 토끼 유래 IgG 항체로, Western blot과 IHC(P) 분석에 적합합니다. 항원 친화 크로마토그래피로 정제되었으며, PBS/glycerol buffer에 보관됩니다. 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 08. 01. 오전 06:10
Thermo Fisher Scientific PA5110612 DKC1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
772,300원VAT 포함 849,530원
Thermo Fisher Scientific PA5110622 DKC1 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
772,300원VAT 포함 849,530원

Thermo Fisher Scientific · Thermo Fisher Scientific DKC1 Polyclonal Antibody

Thermo Fisher Scientific DKC1 Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 0.04–0.4 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant Protein corresponding to Human DKC1. Recombinant protein control fragment (Product #RP-92002).
Conjugate Unconjugated
Form Liquid
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_2856023

Product Specific Information

Immunogen sequence:
EAGTYIRTLC VHLGLLLGVG GQMQELRRVR SGVMSEKDHM VTMHDVLDAQ WLYDNHKDES YLRRVVYPLE KLLTSHKRLV MKDSAVNAIC YGAKIMLPGV LRYEDGIEVN QEIVVIT

Target Information

This gene is a member of the H/ACA snoRNPs gene family. snoRNPs are involved in rRNA processing and modification and are classified into C/D and H/ACA families. The H/ACA snoRNPs include NOLA1, 2, and 3 proteins. The protein encoded by this gene and the NOLA proteins localize to nucleoli and nuclear coiled bodies. Depletion of any of these proteins impairs 18S rRNA production and pseudouridylation. These proteins are also components of the telomerase complex.
Mutations in this gene cause X-linked dyskeratosis congenita and Hoyeraal-Hreidarsson syndrome. Two transcript variants encoding different isoforms have been identified.

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

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