CLCN1 — 카탈로그 5건
Gene CLCN1
NCBI Gene 1180
취급 제조사 2곳
국내 소싱 가능
5건
Stimuli-sensing channels
myotonia congenita, autosomal recessiveThomsen and Becker diseaseMyotoniaTip-toe gaithyperkalemic periodic paralysisAbnormality of the musculatureSmith-Lemli-Opitz syndromegenetic disorder
데이터 출처 · 근거
- NCBI Gene ↗유전자 정보
- Open Targets ↗질환 연관·생물학적 경로
- 대표 논문 (PubMed) Spectrum of mutations in the major human skeletal muscle chloride channel gene (CLCN1) leading to myotonia. · Am J Hum Genet (1995)Myotonia congenita. · Adv Genet (2008)Mutations in the human skeletal muscle chloride channel gene (CLCN1) associated with dominant and recessive myotonia congenita. · Neurology (1996)
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| 견적 | 제조사 | Cat No | Mfr No | 제품명 | Host | Clonality | Reactivity | Application | Size |
|---|---|---|---|---|---|---|---|---|---|
| MyBioSource | R247-173734-01 | MBS7046706 | CLCN1, Polyclonal Antibody | Rabbit | Polyclonal | Human | ELISA; IF | 0.05 mg | |
| Biosynth | F502-135790-01 | 70R-51266 | CLCN1 antibody | Rabbit | Polyclonal | Recognizes endogenous levels of CLCN1 protein; Cross: Mouse, Rat | WB | 100 ul | |
| Biosynth | F502-119306-01 | 70R-16440 | CLCN1 antibody | Rabbit | Polyclonal | Human; Cross: Human, Mouse, Rat | ELISA, WB | 50 ul | |
| Biosynth | F502-138927-01 | 70R-8060 | Clcn1 antibody | Rabbit | Polyclonal | Mouse, Rat; Cross: Predicted: Human, Mouse, Rat, Cow, Dog, Goat, Guinea Pig, Horse, Rabbit | WB | 100 ul |