
Thermo Fisher Scientific PNPase Polyclonal Antibody
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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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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