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Merck
CN

SAB4200289

Sigma-Aldrich

Anti-Dystrobrevin-β (N-terminal) antibody produced in rabbit

~1.5 mg/mL, affinity isolated antibody

别名:

Anti-DTNB

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关于此项目

UNSPSC代码:
12352203
NACRES:
NA.41
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生物来源

rabbit

偶联物

unconjugated

抗体形式

affinity isolated antibody

抗体产品类型

primary antibodies

克隆

polyclonal

表单

buffered aqueous solution

分子量

antigen ~72 kDa

种属反应性

rat, human

浓度

~1.5 mg/mL

技术

immunohistochemistry: 20-40 μg/mL using formalin-fixed, paraffin-embedded rat kidney.
indirect immunofluorescence: 2-4 μg/mL using HEK-293T cells overexpressing human dystrobrevin-β.
western blot: 1.5-3.0 μg/mL using lysates of HEK-293T cells overexpressing human dystrobrevin-β.

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 ... DTNB(1838)
rat ... Dtnb(362715)

一般描述

The dystrobrevin-β(DTNB) gene is mapped to human chromosome 2p23.3. The encoded protein belongs to the dystrobrevin (DB) subfamily of the dystrophin-related protein family. DB is a component of the dystrophin-glycoprotein complex (DGC) that is located at the muscle sarcolemma and forms a transmembrane link between the cytoskeleton and the basal lamina. β-DB is confined to non-muscle tissues and predominantly expressed in the kidney and brain. β-DB is linked to dystrophin and syntrophin isoforms in the hippocampus, cortex, and Purkinje cells. It is abundant in the post-synaptic densities (PSDs).

免疫原

synthetic peptide corresponding to a sequence located at the N-terminus of human dystrobrevin-b (DTNB), conjugated to KLH. The corresponding sequence is identical in human DTNB isoforms 1-5, and highly conserved (single amino acid substitution) in rat and mouse DTNB.

应用

Anti-Dystrobrevin-β (N-terminal) antibody produced in rabbit is suitable for:
  • immunoblotting
  • immunofluorescence
  • immunohistochemistry

生化/生理作用

Anti-Dystrobrevin-b(N-terminal) specifically recognizes human and rat dystrobrevin-b.
Dystrobrevin-β (β-DB) may be significantly involved in assembling and supporting the dystrophin-associated protein complex (DPC)-like complexes in non-muscle tissues. It is known to interact with the neuronal kinesin heavy chain Kif5A and Kif5B in the brain, suggesting that β-DB might act as a motor protein receptor involved in the transport of dystrophin-glycoprotein complex (DGC) components to specific sites in the cell.

外形

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

制备说明

For continuous use, store at 2-8 °C for up to one month. For extended storage, freeze in working aliquots. 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 dilutions should be discarded if not used within 12 hours.

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

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

新产品
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分析证书(COA)

Lot/Batch Number

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P Macioce et al.
Journal of cell science, 116(Pt 23), 4847-4856 (2003-11-06)
Beta-dystrobrevin, a member of the dystrobrevin protein family, is a dystrophin-related and -associated protein restricted to non-muscle tissues and is highly expressed in kidney, liver and brain. Dystrobrevins are now thought to play an important role in intracellular signal transduction
Maria Santa Rocca et al.
European journal of medical genetics, 56(1), 62-65 (2012-11-13)
Deletions of the short arm of chromosome 2 are exceedingly rare and only nine cases involving regions from 2p23 to 2pter have been reported to date. Most of these deletions had only been analysed by GTG banding. Here, we report
T Haenggi et al.
Cellular and molecular life sciences : CMLS, 63(14), 1614-1631 (2006-05-20)
The dystrophin glycoprotein complex (DGC) is a multimeric protein assembly associated with either the X-linked cytoskeletal protein dystrophin or its autosomal homologue utrophin. In striated muscle cells, the DGC links the extracellular matrix to the actin cytoskeleton and mediates three

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