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- pro-1551
- 2026年01月11日
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- 详细信息
- 文献和实验
- 技术资料
- 保存条件：
for future use below -18°C
- 保质期：
See instructions
- 英文名：
BSND
- 库存：
常规产品有备货
- 供应商：
上海经科化学科技有限公司
- CAS号：
无
- 规格：
2ug/10ug/100ug
| 规格： | 2ug | 产品价格： | ￥1080.0 |
|---|---|---|---|
| 规格： | 10ug | 产品价格： | ￥2415.0 |
| 规格： | 100ug | 产品价格： | ￥20286.0 |
CATALOGUE NUMBER
PRO-1551
SYNONYMS
INTRODUCTION
DESCRIPTION
BSND is fused to a 23 amino acid His-tag at N-terminus & purified by proprietary chromatographic techniques.
SOURCE
PHYSICAL APPEARANCE
FORMULATION
STABILITY
For long term storage it is recommended to add a carrier protein (0.1% HSA or BSA).
Avoid multiple freeze-thaw cycles.
PURITY
AMINO ACID SEQUENCE
SAFETY DATA SHEET
SDS
USAGE
ProSpec's products are furnished for LABORATORY RESEARCH USE ONLY. The product may not be used as drugs, agricultural or pesticidal products, food additives or household chemicals.
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文献和实验BSND is a vital beta subunit for CLC chloride channels. These heteromeric channels are restricted to basolateral membranes of renal tubules and of potassium-secreting epithelia of the inner ear. BSND gene mutations are linked with Bartter syndrome with sensorineural deafness.
Discovery Genetics: The History and Future of Spontaneous Mutation Research
.J., Washburn, L.L., Smith, R.S., Andersen, S.G., Swank, R.T., Dell'Angelica, E.C., Bonifacino, J.S., Eicher, E.M., and Peters, L.L. 2000. Defects in the cappuccino (cno) gene on mouse chromosome 5 and human 4p cause Hermansky‐Pudlak syndrome by an AP
Real‐Time Quantitative PCR Analysis of Mitochondrial DNA Content
., Santorelli, F.M., van Rooij, A., Vermunt‐de Koning, D., Morava, E., and Wevers, R.A. 2007. SUCLA2 mutations are associated with mild methylmalonic aciduria, Leigh‐like encephalomyopathy, dystonia and deafness. Brain 130:862‐874
. BONES The human skeleton contains 206 bones, which are composed of inorganic salts (primarily calcium and phosphate), embedded in a framework of collagen fibers. Bone shape and structure Bones are classified
技术资料