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Merck
CN

S8696

Sigma-Aldrich

Anti-Seladin-1 (C-terminal) antibody produced in rabbit

enhanced validation

IgG fraction of antiserum, buffered aqueous solution

别名:

Anti-24-dehydro-cholesterol reductase (DCHR24), Diminuto/Dwarf-1 homolog, Anti-Selective Alzheimer’s Disease Indicator-1

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关于此项目

MDL编号:
UNSPSC代码:
12352203
NACRES:
NA.41
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生物来源

rabbit

偶联物

unconjugated

抗体形式

IgG fraction of antiserum

抗体产品类型

primary antibodies

克隆

polyclonal

表单

buffered aqueous solution

分子量

antigen ~60 kDa

种属反应性

human

增强验证

recombinant expression
Learn more about Antibody Enhanced Validation

技术

western blot: 1:1,000-1:2,000 using HEK293 cells expressing human seladin-1.

UniProt登记号

运输

dry ice

储存温度

−20°C

靶向翻译后修饰

unmodified

基因信息

human ... DYNC1I2(1781)

一般描述

Seladin-1 (C-terminal) is an anti-apoptotic gene, found to be down regulated in large pyramidal neurons in brain regions affected by AD, and to be involved in the regulation of cellular response tooncogenic and oxidative stress.
Selective Alzheimer′s disease indicator-1 (seladin-1) protein is encoded by the 3-β-hydroxysterol-24-reductase (DHCR24) gene. This protein is mainly located in the endoplasmic reticulum. Seladin-1 contains a highly conserved flavin adenine dinucleotide (FAD)-binding domain. DHCR24 gene is located on human chromosome 1p32.3. This gene contains 8 introns and 9 exons.

免疫原

synthetic peptide corresponding to amino acids 505-516 located in a region near the C-terminus of human seladin-1.

应用

Anti-Seladin-1 (C-terminal) antibody produced in rabbit may be used in immunoblotting.

生化/生理作用

Anti-Seladin-1(C-terminal) recognizes human seladin-1.
Selective Alzheimer′s disease indicator-1 (seladin-1) protein catalyzes the conversion of desmosterol to cholesterol. It can protect neurons from β-amyloid toxicity and oxidative stress. In addition, it prevents apoptosis via inhibition of caspase-3, stating that seladin-1 may be involved in the regulation of cell survival and death. Seladin-1 aids to mediate Ras-induced senescence in mouse and human fibroblasts. This protein is upregulated in adrenocortical adenomas and in some tumors. DHCR24 participates plays a key role in cell differentiation, antiapoptotic function, and anti-inflammatory activity. Seladin-1 is known to involve in cholesterol biosynthesis l. A defect in DHCR24 enzyme results in desmosterolosis.

外形

Solution in 0.01 M phosphate buffered saline, pH 7.4, and containing 15 mM sodium azide.

制备说明

For extended storage, freeze in working aliquots at –20 °C. Repeated freezing and thawing, or storage in "frost-free" freezers, is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Working dilution samples should be discarded if not used within 12 hours. For continuous use, store at 2-8 °C for up to one month.

免责声明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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储存分类代码

10 - Combustible liquids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)

法规信息

新产品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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访问文档库

DHCR24 associates strongly with the endoplasmic reticulum beyond predicted membrane domains: implications for the activities of this multi-functional enzyme
Zerenturk EJ, et al.
Bioscience Reports, 34(2), 152-156 (2014)
Regulation of cellular response to oncogenic and oxidative stress by Seladin-1
Wu C, et al.
Nature, 432(2), 640-645 (2004)
DHCR24 predicts poor clinicopathological features of patients with bladder cancer: A STROBE-compliant study
Liu XP, et al.
Medicine, 97(39) (2018)
Desmosterolosis presenting with multiple congenital anomalies
Rohanizadegan M and Sacharow S
European Journal of Medical Genetics, 61(3), 152-156 (2018)

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