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

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Human PNPT1 단백질을 인식하는 Rabbit Polyclonal Antibody로, WB, IHC, ICC/IF에 사용 가능. 항원 친화 크로마토그래피로 정제되었으며, PBS 및 glycerol buffer에 보존. 미토콘드리아 RNA 대사 연구에 적합.

카탈로그번호
PA583236
판매단위
pk
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마지막 업데이트 2025. 07. 31. 오후 03:58
Thermo Fisher Scientific PA583236 PNPase Polyclonal Antibody 100 ul pk판매 단위 pk ·
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740,000원VAT 포함 814,000원

Thermo Fisher Scientific · Thermo Fisher Scientific PNPase Polyclonal Antibody

Applications

Application Tested Dilution
Western Blot (WB) 0.04–0.4 µg/mL
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200
Immunocytochemistry (ICC/IF) 0.25–2 µg/mL

Product Specifications

Specification Description
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human PNPT1. Recombinant protein control fragment (Product #RP-96093).
Conjugate Unconjugated
Form Liquid
Concentration 0.3 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 40% glycerol
Contains 0.02% 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_2790392

Product Specific Information

Immunogen sequence:
FSVFAPTPSA MHEARDFITE ICKDDQEQQL EFGAVYTATI TEIRDTGVMV KLYPNMTAVL LHNTQLDQRK IKHPTALGLE VGQEIQVKYF GRDPA

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. It plays roles in cytoplasmic RNA import, mitochondrial morphogenesis and respiration, regulation of electron transport chain expression, stability of mature miRNAs in melanoma cells, and RNA surveillance. Mutations can result in combined oxidative phosphorylation deficiency 13 (COXPD13) and autosomal recessive deafness (DFNB70).

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

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