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Merck

RAB1708

Sigma-Aldrich

人SMPD1 ELISA

for serum, plasma and cell culture supernatants

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About This Item

UNSPSC代码:
41116158
NACRES:
NA.32

种属反应性

human

技术

ELISA: suitable

assay range

inter-assay cv: <12%
intra-assay cv: <10%

运输

wet ice

储存温度

−20°C

一般描述

Sphingomyelin phosphodiesterase-1 (SMPD1) gene encodes for acid sphingomyelinase (aSMase), which is involved in the hydrolysis of sphingomyelin to ceramides and phosphorylcholine in the late endosomes and lysosomes. Ceramides act as proinflammatory and proapoptotic second messengers. Mutations in the SMPD1 gene are associated with a lack of aSMase, leading to Niemann-Pick disease type A and B. The SMPD1 gene is mapped to the human chromosome at 11p15.1–11p15.4.

应用

For research use only. Not for use in diagnostic procedures.
Please refer to the attached Protocolfor details.

其他说明

A sample Certificate of Analysis is available for this product. Please type the word sample in the text box provided for lot number.

象形图

Corrosion

警示用语:

Warning

危险声明

预防措施声明

危险分类

Met. Corr. 1

储存分类代码

8A - Combustible corrosive hazardous materials

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Compound heterozygosity at the sphingomyelin phosphodiesterase-1 (SMPD1) gene is associated with low HDL cholesterol
Ching Y L, et al.
Human Genetics, 552?562-552?562 (2003)
Analysis of the sphingomyelin phosphodiesterase 1 gene (SMPD1) in Turkish Niemann?Pick disease patients: Mutation profile and description of a novel mutation
Ayukt A, et al.
Gene, 484-486 (2013)
Sphingomyelin phosphodiesterase 1 (SMPD1) mediates the attenuation of myocardial infarction-induced cardiac fibrosis by astaxanthin
Yu S, et al.
Biochemical and Biophysical Research Communications, 503(2), 637-643 (2018)

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