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Merck
CN

NE1015

Sigma-Aldrich

Anti-Glial Fibrillary Acidic Protein Cocktail Mouse mAb (SMI-22)

liquid, clone SMI-22, Calbiochem®

别名:

Anti-GFAP Cocktail

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关于此项目

UNSPSC代码:
12352203
NACRES:
NA.43
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生物来源

mouse

质量水平

抗体形式

ascites fluid

抗体产品类型

primary antibodies

克隆

SMI-22, monoclonal

表单

liquid

包含

≤0.1% sodium azide as preservative

种属反应性

human, bovine, mouse, guinea pig, porcine, sheep, canine, rat, chicken

制造商/商品名称

Calbiochem®

储存条件

OK to freeze
avoid repeated freeze/thaw cycles

dilution

(ELISA (1:1000)
Frozen Sections (1:1000)
Immunoblotting (1:1000)
Immunocytochemistry (1:1000)
Paraffin Sections (1:1000, trypsin or heat pre-treatment required))

同位素/亚型

IgG2b

运输

wet ice

储存温度

−20°C

靶向翻译后修饰

unmodified

基因信息

human ... GFAP(2670)

一般描述

Mouse monoclonal antibody cocktail that contains a mixture of 3 antibodies supplied as undiluted ascites. Recognizes the ~50 kDa glial fibrillary acidic protein.
Recognizes ~50 kDa glial fibrillary acidic protein (GFAP) in human and bovine cytoskeletal preparations.
This Anti-Glial Fibrillary Acidic Protein Cocktail Mouse mAb is validated for use in ELISA, Frozen Sections, WB, ICC, Paraffin Sections for the detection of Glial Fibrillary Acidic Protein.

免疫原

Bovine
purified bovine GFAP protein

应用




ELISA (1:1000)
Frozen Sections (1:1000, see comments)
Immunoblotting (1:1000)
Immunocytochemistry (1:1000, see comments)
Paraffin Sections (1:1000, trypsin or heat pre-treatment required)

外形

Undiluted ascites.

制备说明

Upon initial thaw, aliquot and freeze (-20°C).

分析说明

Positive Control
Astrocytes or cytoskeletal preparations

其他说明

This cocktail is derived from the Bigner-Eng clones MAb1B4, MAb2E1, and MAb4A11 and provides a means for more comprehensive detection of astrocytomas than each clone alone. Each component is specific for GFAP and stains astrocytes and astrocytic processes as well as Bergman glia. Recognizes both anaplastic and reactive astrocytes by immunocytochemical staining. Does not recognize metastatic tumors and brain tumors of non-astrocytic origin, including medulloblastomas, meningiomas, choroid plexus papillomas, and schwannomas. For staining paraffin sections it is recommended that de-paraffinized sections be treated with 0.1% trypsin in 50 mM Tris-HCl, pH 7.6 for 20-30 min at 37°C or boiled in Tris-buffered saline, pH 9.0 for 15 min to expose the epitope. For immunocytochemistry or staining frozen sections, post-fixation in cold methanol or methanol/hydrogen peroxide for 10 min is required for access to the astrocytes in the sample. Antibody should be titrated for optimal results in individual systems.
Vick, W.W., et al. 1987. Acta. Cytol.31, 816.
McLendon R.E., et al. 1986. J. Neuropathol. Exp. Neurol.45, 692.
Pegram, C.N., et al. 1985. Neurochem. Pathol.3, 119.

法律信息

CALBIOCHEM is a registered trademark of Merck KGaA, Darmstadt, Germany

免责声明

Toxicity: Standard Handling (A)

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储存分类代码

10 - Combustible liquids

WGK

WGK 1


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