SLC26A4 — 카탈로그 9건
Gene SLC26A4
NCBI Gene 5172
국내 소싱 가능
9건
Defective SLC26A4 causes Pendred syndrome (PDS)Inorganic anion exchange by SLC26 transporters
Pendred syndromeautosomal recessive nonsyndromic hearing loss 4hearing loss, autosomal recessivedeafnessRare genetic deafnessHearing impairmentsensorineural hearing lossSensorineural hearing impairment
데이터 출처 · 근거
- NCBI Gene ↗유전자 정보
- Open Targets ↗질환 연관·생물학적 경로
- 대표 논문 (PubMed) Ethnic-specific spectrum of GJB2 and SLC26A4 mutations: their origin and a literature review. · Ann Otol Rhinol Laryngol (2015)Functional characterization of wild-type and mutated pendrin (SLC26A4), the anion transporter involved in Pendred syndrome. · J Mol Endocrinol (2009)Molecular epidemiology and functional assessment of novel allelic variants of SLC26A4 in non-syndromic hearing loss patients with enlarged vestibular aqueduct in China. · PLoS One (2012)
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 | T094-107122-01 | CSB-PA021527LA01HU | SLC26A4 Antibody | Rabbit | Polyclonal | Human | ELISA, WB, IHC, IF | 50μg, 100μg | |
| Cloud-Clone | T813-125845-01 | PAE474Hu01 | Polyclonal Antibody to Solute Carrier Family 26, Member 4 (SLC26A4) | Rabbit | Polyclonal | Human | WB; IHC; ICC; IP. | 100µl | |
| Cloud-Clone | T813-114772-01 | MAE474Hu21 | Monoclonal Antibody to Solute Carrier Family 26, Member 4 (SLC26A4) | Mouse | Monoclonal | Human | WB; IHC; ICC; IP. | 100µl | |
| Biosynth | F502-138185-01 | 70R-7041 | SLC26A4 antibody | Rabbit | Polyclonal | SLC26A4 antibody was raised against the middle region of SLC26A4; Cross: Human,Mouse | WB | 100 ul |