NR2E3 — 카탈로그 4건
Gene NR2E3
NCBI Gene 10002
취급 제조사 3곳
국내 소싱 가능
4건
Nuclear Receptor transcription pathway
enhanced S-cone syndromeretinitis pigmentosa 37retinitis pigmentosaGoldmann-Favre syndromeRetinal dystrophyhemoglobin measurementJoubert syndrome and related disorderssitting height measurement
데이터 출처 · 근거
- NCBI Gene ↗유전자 정보
- Open Targets ↗질환 연관·생물학적 경로
- 대표 논문 (PubMed) The nuclear receptor NR2E3 plays a role in human retinal photoreceptor differentiation and degeneration. · Proc Natl Acad Sci U S A (2002)Nuclear receptor NR2E3 gene mutations distort human retinal laminar architecture and cause an unusual degeneration. · Hum Mol Genet (2004)NR2E3 mutations in enhanced S-cone sensitivity syndrome (ESCS), Goldmann-Favre syndrome (GFS), clumped pigmentary retinal degeneration (CPRD), and retinitis pigmentosa (RP). · Hum Mutat (2009)
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 |
|---|---|---|---|---|---|---|---|---|---|
| Cusabio | T094-108776-01 | CSB-PA865585LA01HU | NR2E3 Antibody | Rabbit | Polyclonal | Human | ELISA, IHC | 50μg, 100μg | |
| Biosynth | F502-122034-01 | 70R-18953 | NR2E3 antibody | Rabbit | Polyclonal | Human; Cross: Human, Mouse, Rat | ELISA, IHC, WB | 50 ul |