SCO2 — 카탈로그 6건
Gene SCO2
NCBI Gene 9997
국내 소싱 가능
6건
Complex IV assemblyTP53 Regulates Metabolic Genes
cardioencephalomyopathy, fatal infantile, due to cytochrome c oxidase deficiency 1myopia 6fatal infantile encephalocardiomyopathyRare isolated myopiamitochondrial DNA depletion syndrome 1mitochondrial diseaseneurodegenerative diseasemitochondrial neurogastrointestinal encephalomyopathy
데이터 출처 · 근거
- NCBI Gene ↗유전자 정보
- Open Targets ↗질환 연관·생물학적 경로
- 대표 논문 (PubMed) Copper metabolism in cell death and autophagy. · Autophagy (2023)The molecular mechanisms of copper metabolism and its roles in human diseases. · Pflugers Arch (2020)Human SCO1 and SCO2 have independent, cooperative functions in copper delivery to cytochrome c oxidase. · Hum Mol Genet (2004)
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 | F502-123303-01 | 70R-20118 | SCO2 antibody | Rabbit | Polyclonal | Human; Cross: Human, Mouse | ELISA, IHC, WB | 50 ul | |
| Cloud-Clone | T813-128198-01 | PAM192Hu01 | Polyclonal Antibody to SCO Cytochrome Oxidase Deficient Homolog 2 (SCO2) | Rabbit | Polyclonal | Human | WB; IHC | 100µl | |
| MyBioSource | R247-134864-01 | MBS240375 | SCO2, Polyclonal Antibody | Rabbit | Polyclonal | Human | Immunohistochemistry (IHC - Paraffin); WB | ||
| ELK Biotechnology | T376-115219-01 | ES11415 | SCO2 rabbit pAb | Rabbit | Polyclonal | Human;Mouse | WB;ELISA | 50μL |