MPV17 — 카탈로그 3건
Gene MPV17
NCBI Gene 4358
취급 제조사 2곳
국내 소싱 가능
3건
Peroxisomal protein import
mitochondrial DNA depletion syndrome 6 (hepatocerebral type)Charcot-Marie-Tooth disease, axonal, type 2EEmitochondrial DNA depletion syndromemitochondrial DNA depletion syndrome 15 (hepatocerebral type)mitochondrial diseaseliver failureHepatic failureCholestasis
데이터 출처 · 근거
- NCBI Gene ↗유전자 정보
- Open Targets ↗질환 연관·생물학적 경로
- 대표 논문 (PubMed) Mitochondrial DNA depletion syndromes: review and updates of genetic basis, manifestations, and therapeutic options. · Neurotherapeutics (2013)Mitochondrial DNA maintenance defects. · Biochim Biophys Acta Mol Basis Dis (2017)Mitochondrial myopathies. · Curr Opin Rheumatol (2006)
체크박스로 여러 제품을 선택해 한 번에 견적을 요청하세요. 제조사·Cat No·Application을 한 표에서 비교합니다.
| 견적 | 제조사 | Cat No | Mfr No | 제품명 | Host | Clonality | Reactivity | Application | Size |
|---|---|---|---|---|---|---|---|---|---|
| Biosynth | F502-121631-01 | 70R-18584 | MPV17 antibody | Rabbit | Polyclonal | Human; Cross: Human, Mouse, Rat | ELISA, IHC, WB | 50 ul | |
| ELK Biotechnology | T376-117042-01 | ES14715 | MPV17 rabbit pAb | Rabbit | Polyclonal | Human; Mouse;Rat | WB | 50μL |