CacheBy
Thermo Fisher Scientific PNPase Recombinant Rabbit Monoclonal Antibody (24H24L10)
원본

Thermo Fisher Scientific PNPase Recombinant Rabbit Monoclonal Antibody (24H24L10)

상품 한눈에 보기

PNPase 단백질을 인식하는 재조합 토끼 단클론 항체로, Western blot 및 면역세포염색에 적합합니다. 인간에 반응하며, 마우스·랫·소에서도 예측 반응합니다. 고순도 Protein A 정제, 액상 형태로 제공되며 안정적 보관이 가능합니다.

판매단위
pk
카탈로그 보기

카탈로그

1개 옵션
회원가입 없이 바로 구매하세요
가입하지 않아도 비회원가로 구매하실 수 있습니다.
마지막 업데이트 2025. 08. 05. 오후 01:33
Thermo Fisher Scientific 703101 PNPase Recombinant Rabbit Monoclonal Antibody (24H24L10) 100 ug pk판매 단위 pk ·
재고 확인 필요
614,900원VAT 포함 676,390원

Thermo Fisher Scientific · Thermo Fisher Scientific PNPase Recombinant Rabbit Monoclonal Antibody (24H24L10)

Applications

Western Blot (WB)

  • Tested Dilution: 1:500

Immunocytochemistry (ICC/IF)

  • Tested Dilution: 1:100 – 1:500

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Expression System Expi293
Class Recombinant Monoclonal
Type Antibody
Clone 24H24L10
Immunogen Protein corresponding to human PNPase (aa46–aa669)
Conjugate Unconjugated
Form Liquid
Concentration 0.5 mg/mL
Purification Protein A
Storage Buffer PBS, pH 7.4
Contains 0.09% 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_2809225

Product Specific Information

This antibody is predicted to react with Mouse, Rat, and Bovine.

Target Information

PNPT1 (polyribonucleotide nucleotidyltransferase 1, mitochondrial) is an RNA-binding protein implicated in numerous RNA metabolic processes. It catalyzes the phosphorolysis of single-stranded polyribonucleotides processively in the 3′-to-5′ direction. PNPT1 is a component of the mitochondrial degradosome (mtEXO) complex that degrades 3′ overhang double-stranded RNA in an ATP-dependent manner. It is required for correct processing and polyadenylation of mitochondrial mRNAs. Additionally, it plays roles in cytoplasmic RNA import, mitochondrial morphogenesis, respiration, electron transport chain expression regulation, miRNA stability, and RNA surveillance. Mutations can lead to combined oxidative phosphorylation deficiency 13 (COXPD13) and autosomal recessive deafness 70 (DFNB70).


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

Thermo Fisher Scientific 상품 둘러보기

전체보기

문의

0

아직 등록된 문의가 없어요.