EHHADH — 카탈로그 6건
Gene EHHADH
NCBI Gene 1962
취급 제조사 3곳
국내 소싱 가능
6건
Beta-oxidation of very long chain fatty acidsPeroxisomal protein import
primary Fanconi syndromeFanconi renotubular syndrome 1body mass indexbody weightd-bifunctional protein deficiencysex hormone-binding globulin measurementinsomniacardiac arrest
데이터 출처 · 근거
- NCBI Gene ↗유전자 정보
- Open Targets ↗질환 연관·생물학적 경로
- 대표 논문 (PubMed) Regulation of cellular metabolism by protein lysine acetylation. · Science (2010)TXNIP/VDUP1 attenuates steatohepatitis via autophagy and fatty acid oxidation. · Autophagy (2021)Mistargeting of peroxisomal EHHADH and inherited renal Fanconi's syndrome. · N Engl J Med (2014)
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| 견적 | 제조사 | Cat No | Mfr No | 제품명 | Host | Clonality | Reactivity | Application | Size |
|---|---|---|---|---|---|---|---|---|---|
| Cusabio | T094-107595-01 | CSB-PA600104LA01HU | EHHADH Antibody | Rabbit | Polyclonal | Human, Mouse | ELISA, WB, IHC | 50μg, 100μg | |
| Biosynth | F502-134067-01 | 70R-49693 | EHHADH antibody | Rabbit | Polyclonal | Recognizes endogenous levels of EHHADH protein; Cross: Mouse, Rat | WB, IHC | 100 ul |