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Merck
CN

G9152

Sigma-Aldrich

抗 半乳糖脑苷脂 兔抗

whole antiserum

别名:

Galactocerebroside Antibody, Galactocerebroside Antibody - Anti-Galactocerebroside antibody produced in rabbit

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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

质量水平

偶联物

unconjugated

抗体形式

whole antiserum

抗体产品类型

primary antibodies

克隆

polyclonal

包含

15 mM sodium azide

种属反应性

human

技术

dot blot: 1:50 using galactocerebroside I and II

运输

dry ice

储存温度

−20°C

靶向翻译后修饰

unmodified

一般描述

Galactocerebroside is the major galactosphingolipid of myelin. It is expressed in the CNS in cell membranes of oligodendrocytes. It is also expressed in Schwann cells in peripheral nerves.
This product is a pooled delipidized antiserum produced in rabbits by repeated injections of a mixture of galactocerebrosides I and II conjugated to keyhole limpet hemocyanin.

免疫原

Galactocerebrosides (GalC) I and II conjugated to KLH

应用

Anti-Galactocerebroside antibody produced in rabbit has been used:
  • for dot-blot immunoassay and western blot analysis of mouse brain homogenates
  • as a primary antibody at a working dilution of 1:50 for immunostaining of muscle tissue of Rana pipiens frogs
  • as a primary antibody at a working dilution of 1:500 in immunofluorescence and immunohistochemistry using primary human astroglia

生化/生理作用

Galactocerebroside is the major galactosphingolipid of myelin. It is expressed in the CNS in cell membranes of oligodendrocytes. It is also expressed in Schwann cells in peripheral nerves. Galactocerebroside is found in serum and cerebral spinal fluid of patients with demyelinating diseases like multiple sclerosis.
Galactocerebroside was shown to play an important role in the processes of normal development and myelination and is known to be an early marker of oligodendrocyte development.
The antibody localizes oligodendroglia in cultured cells. It may be used for studying changes in the organization of oligodendroglial membrane sheets in culture. Specificity of the product is determined by dot blotting using galactocerebroside as the antigen.

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

法规信息

常规特殊物品
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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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Lead alters the developmental profile of the galactolipid metabolic enzymes in cultured oligodendrocyte lineage cells
Deng W and Poretz RD
Neurotoxicology, 22(4), 429-437 (2001)
B Zalc et al.
Brain research, 211(2), 341-354 (1981-05-04)
We have used purified antibodies against galactosylceramide (galCb) and sulfogalactosylceramide (sulf) to study the topographical distribution of these two lipid haptens in the brain of the 30-day-old mouse. This study has been conducted, using the indirect immunofluorescence method, on cerebellum
J W Prineas et al.
Laboratory investigation; a journal of technical methods and pathology, 61(5), 489-503 (1989-11-01)
Fresh lesions in the brain and spinal cord of patients with multiple sclerosis who died shortly after the onset of symptoms were examined immunocytochemically for myelin and oligodendrocyte antigens that are known to be sequentially expressed during normal development. Cells
C A Dyer et al.
The Journal of neuroscience : the official journal of the Society for Neuroscience, 8(11), 4307-4318 (1988-11-01)
Antibodies to galactocerebroside (GalC) cause major changes in the organization of the membrane sheets elaborated by murine oligodendroglia in culture. Exposure of oligodendroglia to rabbit anti-GalC IgG for 15 min followed by fluoresceinated second antibodies results in patches of surface
D M Kokkinakis et al.
Neuro-oncology, 3(2), 99-112 (2001-04-12)
Glial tumors may originate from the malignant transformation of multipotent glial progenitor cells, but tools to study malignant transformation leading to gliomas are limited by the lack of biological systems that represent early stages of this disease in adult animals.

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