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

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PNPase 단백질을 인식하는 Rabbit Polyclonal Antibody로, 인간 및 마우스 시료에 반응합니다. Western blot, IHC, ICC/IF 등 다양한 응용에 적합하며 고순도 Affinity chromatography로 정제되었습니다. PBS와 50% glycerol buffer에 보관되며 -20°C에서 안정적으로 저장 가능합니다.

카탈로그번호
PA5115776
판매단위
pk
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마지막 업데이트 2025. 08. 02. 오전 03:20
Thermo Fisher Scientific PA5115776 PNPase Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
655,000원VAT 포함 720,500원

Thermo Fisher Scientific · Thermo Fisher Scientific PNPase Polyclonal Antibody

Applications

Application Tested Dilution
Western Blot (WB) 1:1,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200
Immunocytochemistry (ICC/IF) 1:100–1:500

Product Specifications

Specification Description
Species Reactivity Human, Mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen A synthesized peptide derived from human PNPT1 (Accession Q8TCS8), corresponding to amino acid residues K716–R766
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Affinity chromatography
Storage Buffer PBS with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions -20°C
Shipping Conditions Wet ice
RRID AB_2900411

Product Specific Information

Antibody detects endogenous levels of total PNPase.

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 with a 3′-to-5′ directionality in an ATP-dependent manner. It is required for correct processing and polyadenylation of mitochondrial mRNAs. PNPT1 also plays roles in cytoplasmic RNA import, mitochondrial morphogenesis and respiration, regulation of electron transport chain expression, stability of specific mature miRNAs in melanoma cells, and RNA surveillance. Mutations in this gene can result in 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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