GJB3 — 카탈로그 3건
Gene GJB3
NCBI Gene 2707
취급 제조사 2곳
국내 소싱 가능
3건
Differentiation of Keratinocytes in Interfollicular Epidermis in Mammalian SkinGap junction assembly
erythrokeratodermia variabilisautosomal dominant nonsyndromic hearing lossdeafnesshearing loss, autosomal recessiveautosomal recessive nonsyndromic hearing loss 1Aperipheral neuropathyerythrokeratodermaPeripheral neuropathy
데이터 출처 · 근거
- NCBI Gene ↗유전자 정보
- Open Targets ↗질환 연관·생물학적 경로
- 대표 논문 (PubMed) Mutations in the gene encoding gap junction protein beta-3 associated with autosomal dominant hearing impairment. · Nat Genet (1998)Mutations in the human connexin gene GJB3 cause erythrokeratodermia variabilis. · Nat Genet (1998)Connexins: a connection with the skin. · Exp Dermatol (2000)
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 | T094-105820-01 | CSB-PA009453LA01HU | GJB3 Antibody | Rabbit | Polyclonal | Human | ELISA, WB, IF | 50μg, 100μg | |
| MyBioSource | R247-213724-01 | MBS9607767 | GJB3, Polyclonal Antibody | Rabbit | Polyclonal | Human, Mouse, Rat | WB; IHC; ELISA | 0.1 mL |