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Merck
CN
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文件

安全信息

HPA030741

Sigma-Aldrich

Anti-CCNB1 antibody produced in rabbit

enhanced validation

Prestige Antibodies® Powered by Atlas Antibodies, affinity isolated antibody

别名:

CCNB

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About This Item

UNSPSC代码:
12352203
人类蛋白质图谱编号:
NACRES:
NA.43

生物来源

rabbit

质量水平

偶联物

unconjugated

抗体形式

affinity isolated antibody

抗体产品类型

primary antibodies

克隆

polyclonal

产品线

Prestige Antibodies® Powered by Atlas Antibodies

形式

buffered aqueous glycerol solution

种属反应性

human

增强验证

RNAi knockdown
Learn more about Antibody Enhanced Validation

技术

immunoblotting: 0.04-0.4 μg/mL
immunofluorescence: 0.25-2 μg/mL

免疫原序列

PVPVSEPVPEPEPEPEPEPVKEEKLSPEPILVDTASPSPMETSGCAPAEEDLCQAFSDVILAVNDVDAEDGAD

UniProt登记号

运输

wet ice

储存温度

−20°C

靶向翻译后修饰

unmodified

基因信息

human ... CCNB1(891)

一般描述

G2/mitotic-specific cyclin-B1 (CCNB1), also known as cyclin B1, regulates cell division in eukaryotes. It has N-terminal and C-terminal cyclin box motifs. CCNB1 is located on human chromosome 5q13.

免疫原

cyclin B1

应用

All Prestige Antibodies Powered by Atlas Antibodies are developed and validated by the Human Protein Atlas (HPA) project and as a result, are supported by the most extensive characterization in the industry.

The Human Protein Atlas project can be subdivided into three efforts: Human Tissue Atlas, Cancer Atlas, and Human Cell Atlas. The antibodies that have been generated in support of the Tissue and Cancer Atlas projects have been tested by immunohistochemistry against hundreds of normal and disease tissues and through the recent efforts of the Human Cell Atlas project, many have been characterized by immunofluorescence to map the human proteome not only at the tissue level but now at the subcellular level. These images and the collection of this vast data set can be viewed on the Human Protein Atlas (HPA) site by clicking on the Image Gallery link. We also provide Prestige Antibodies® protocols and other useful information.

生化/生理作用

Cyclin B1 (CCNB1) interacts with cyclin B1−associated kinase (Cdk1) and coordinates mitotic cycle events. CCNB1 is crucial for maintenance of cell division and arrest in the presence of antineoplastic agents. It is highly expressed in breast and small cell lung cancer. CCNB1 may play a key role in pathogenesis of pituitary adenomas.

特点和优势

Prestige Antibodies® are highly characterized and extensively validated antibodies with the added benefit of all available characterization data for each target being accessible via the Human Protein Atlas portal linked just below the product name at the top of this page. The uniqueness and low cross-reactivity of the Prestige Antibodies® to other proteins are due to a thorough selection of antigen regions, affinity purification, and stringent selection. Prestige antigen controls are available for every corresponding Prestige Antibody and can be found in the linkage section.

Every Prestige Antibody is tested in the following ways:
  • IHC tissue array of 44 normal human tissues and 20 of the most common cancer type tissues.
  • Protein array of 364 human recombinant protein fragments.

联系

Corresponding Antigen APREST89285

外形

Solution in phosphate buffered saline, pH 7.2, containing 40% glycerol and 0.02% sodium azide.

法律信息

Prestige Antibodies is a registered trademark of Merck KGaA, Darmstadt, Germany

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WGK

WGK 1

闪点(°F)

Not applicable

闪点(°C)

Not applicable

法规信息

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分析证书(COA)

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在文件库中查找您最近购买产品的文档。

访问文档库

The roles of cyclin A2, B1, and B2 in early and late mitotic events
Gong D and Ferrell JE Jr
Molecular Biology of the Cell, 21(18), 3149-3161 (2010)
Nuclear cyclin B1 in human breast carcinoma as a potent prognostic factor
Suzuki T, et al.
Cancer Science, 98(5), 644-651 (2007)
Overexpression of cyclin B1 in early-stage non-small cell lung cancer and its clinical implication
Soria JC, et al.
Cancer Research, 60(15), 4000-4004 (2000)
Human cyclin B1 gene (CCNB1) assigned to chromosome 5 (q13-qter)
Milatovich A and Francke U
Somatic Cell and Molecular Genetics, 18(3), 303-307 (1992)
The crystal structure of human cyclin B
Petri ET, et al.
Cell Cycle, 6(11), 1342-1349 (2007)

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