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Thermo Fisher Scientific PNPase Monoclonal Antibody (3H5)
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Thermo Fisher Scientific PNPase Monoclonal Antibody (3H5)

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Thermo Fisher Scientific의 PNPase Monoclonal Antibody (3H5)는 인간 PNPase를 인식하는 Mouse IgG1 단일클론 항체입니다. ICC/IF에 적합하며, Protein G로 정제된 액상 제품입니다. PBS와 20% glycerol에 보관되며, 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 08. 05. 오전 04:12
Thermo Fisher Scientific MA527858 PNPase Monoclonal Antibody (3H5) 100 ul pk판매 단위 pk ·
재고 확인 필요
731,200원VAT 포함 804,320원

Thermo Fisher Scientific · Thermo Fisher Scientific PNPase Monoclonal Antibody (3H5)

Applications and Tested Dilution

Application Tested Dilution
Immunocytochemistry (ICC/IF) 1:100–1:1,000

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone 3H5
Immunogen Human PNPase
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein G
Storage Buffer PBS with 20% glycerol
Contains No preservative
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Ambient (domestic); Wet ice (international)
RRID AB_2735324

Product Specific Information

Store product as a concentrated solution. Centrifuge briefly prior to opening the vial.

Target Information

PNPT1 (polyribonucleotide nucleotidyltransferase 1, mitochondrial) is an RNA-binding protein involved in multiple RNA metabolic processes. It catalyzes the phosphorolysis of single-stranded polyribonucleotides in the 3′-to-5′ direction and is a component of the mitochondrial degradosome (mtEXO) complex that degrades double-stranded RNA with 3′ overhangs in an ATP-dependent manner. PNPT1 is essential for proper processing and polyadenylation of mitochondrial mRNAs. It also functions as a cytoplasmic RNA import factor, contributing to mitochondrial morphogenesis, respiration, and regulation of electron transport chain expression. Additionally, it influences the stability of specific mature miRNAs in melanoma cells and participates in RNA surveillance. Mutations in this gene can cause 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.

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