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Thermo Fisher Scientific PNPase Polyclonal Antibody
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Thermo Fisher Scientific PNPase Polyclonal Antibody

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Rabbit polyclonal antibody targeting human PNPase (PNPT1). Validated for WB and IP applications. Predicted cross-reactivity with mouse. Supplied as liquid, 1 mg/mL, stored at 4°C. For research use only.

판매단위
pk
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Thermo Fisher Scientific A303917AM PNPase Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
477,300원VAT 포함 525,030원
Thermo Fisher Scientific A303917AT PNPase Polyclonal Antibody 10 ul pk판매 단위 pk ·
재고 확인 필요
194,600원VAT 포함 214,060원

Thermo Fisher Scientific · Thermo Fisher Scientific PNPase Polyclonal Antibody

Applications

Application Tested Dilution
Western Blot (WB) 1:1,000–1:5,000
Immunoprecipitation (IP) 2–10 µg/mg lysate

Product Specifications

Specification Description
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Region between residue 700 and 750 of Human Polynucleotide Phosphorylase 1 (PNPase)
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Storage Conditions 4°C
Shipping Conditions Wet ice

Product Specific Information

The recommended shelf life for this product is 1 year from date of receipt.
Based on 100% sequence identity, this antibody is predicted to react with Mouse.

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 processively in the 3′-to-5′ direction. PNPT1 is a component of the mitochondrial degradosome (mtEXO) complex that degrades double-stranded RNA with 3′ overhangs in an ATP-dependent manner. It is required for proper processing and polyadenylation of mitochondrial mRNAs.
PNPT1 also functions as a cytoplasmic RNA import factor, plays roles in mitochondrial morphogenesis, respiration, and regulation of electron transport chain expression. It contributes to the stability of specific mature miRNAs in melanoma cells and RNA surveillance.
Mutations in this gene are associated with 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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