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Thermo Fisher Scientific ZNF408/PRDM17 (Transcription Factor) Monoclonal Antibody (PCRP-ZNF408-1E5)
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Thermo Fisher Scientific ZNF408/PRDM17 (Transcription Factor) Monoclonal Antibody (PCRP-ZNF408-1E5)

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ZNF408/PRDM17 전사인자에 특이적인 Thermo Fisher Scientific의 단클론 항체입니다. Western blot, 유세포분석, 펩타이드 어레이 등에 적합하며, 인간 시료 반응성을 가집니다. 단백질 A/G 정제, 액상 형태로 제공되며 4°C에서 보관합니다.

카탈로그번호
79797-MSM1-P0
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 09:58
Thermo Fisher Scientific 79797-MSM1-P0 ZNF408/PRDM17 (Transcription Factor) Monoclonal Antibody (PCRP-ZNF408-1E5) 20 ug pk판매 단위 pk ·
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441,900원VAT 포함 486,090원

Thermo Fisher Scientific · Thermo Fisher Scientific ZNF408/PRDM17 (Transcription Factor) Monoclonal Antibody (PCRP-ZNF408-1E5)

Applications

Application Tested Dilution
Western Blot (WB) 1–2 µg/mL
Flow Cytometry (Flow) 1–2 µg/10⁶ cells
Peptide Array (Array) Assay-dependent

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2b
Class Monoclonal
Type Antibody
Clone PCRP-ZNF408-1E5
Immunogen Recombinant full-length human ZNF408 protein (amino acids 1–720)
Conjugate Unconjugated
Form Liquid
Concentration 200 µg/mL
Purification Protein A/G
Storage Buffer PBS, pH 7.4, with 0.05% BSA
Contains 0.05% sodium azide
Storage Conditions 4°C
Shipping Conditions Ambient (domestic); Wet ice (international)

Target Information

Zinc-finger proteins contain DNA-binding domains and perform diverse functions, including transcriptional activation or repression. Most zinc-finger proteins have a Kruppel-type DNA-binding domain and a KRAB domain that interacts with KAP1 to recruit histone-modifying proteins.
ZNF408 (also known as PRDM17) is a member of the Kruppel C2H2-type zinc-finger protein family. It is a 720-amino-acid nuclear protein containing 10 C2H2-type zinc fingers. The ZNF408 gene maps to human chromosome 11, which contains over 1,400 genes and represents nearly 4% of the human genome. Mutations in genes on chromosome 11 are associated with disorders such as Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema, and Smith-Lemli-Opitz syndrome.


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

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