RPGRIP1L — 카탈로그 3건
Gene RPGRIP1L
NCBI Gene 23322
취급 제조사 2곳
국내 소싱 가능
3건
Anchoring of the basal body to the plasma membraneHedgehog 'off' state
Joubert syndromeJoubert syndrome with hepatic defectMeckel syndromeMeckel syndrome, type 5Joubert syndrome 7Joubert syndrome and related disordersgenetic disorderciliopathy
데이터 출처 · 근거
- NCBI Gene ↗유전자 정보
- Open Targets ↗질환 연관·생물학적 경로
- 대표 논문 (PubMed) The ciliary gene RPGRIP1L is mutated in cerebello-oculo-renal syndrome (Joubert syndrome type B) and Meckel syndrome. · Nat Genet (2007)Hypomorphism for RPGRIP1L, a ciliary gene vicinal to the FTO locus, causes increased adiposity in mice. · Cell Metab (2014)Genotype-phenotype correlates in Joubert syndrome: A review. · Am J Med Genet C Semin Med Genet (2022)
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 | F502-123128-01 | 70R-19957 | RPGRIP1L antibody | Rabbit | Polyclonal | Human; Cross: Human | ELISA, WB | 50 ul | |
| MyBioSource | R247-176766-01 | MBS712768 | RPGRIP1-like (RPGRIP1L), Polyclonal Antibody | Rabbit | Polyclonal | Human | ELISA; WB | 0.1 mL |