BEND2蛋白抗体elisa实验|0.1ml/100μg 0.2ml/200μg|BJ-3819-上海邦景实业有限公司

BEND2蛋白抗体elisa实验

参考价：面议

供货周期：

现货

品牌：

GenWay

规格：

0.1ml/100μg 0.2ml/200μg

货号：

BJ-3819

CAS号：

产品详情

BEND2蛋白抗体英文名称 Anti-BEND2/CXorf56

中文名称 BEND2蛋白抗体

别名 BEN domain-containing protein 2; BEN domain containing 2; BEND 2; BEND2; BEND-2; Chromosome X open reading frame 20; MGC33653; BEND2_HUMAN.

浓度 1mg/1ml

规格 0.2ml/200μg

抗体来源 Rabbit

BEND2蛋白抗体克隆类型 polyclonal

交叉反应 Human

产品类型一抗

研究领域细胞生物发育生物学

蛋白分子量 predicted molecular weight: 88kDa

性状 Lyophilized or Liquid

免疫原 KLH conjugated synthetic peptide derived from human BEND2/CXorf56

亚型 IgG

纯化方法 affinity purified by Protein A

储存液 Preservative: 15mM Sodium Azide, Constituents: 1% BSA, 0.01M PBS, pH 7.4

产品应用 WB=1:100-500 ELISA=1:500-1000 IHC-P=1:100-500 IHC-F=1:100-500 ICC=1:100-500 IF=1:100-500

（石蜡切片需做抗原修复）

not yet tested in other applications.

optimal dilutions/concentrations should be determined by the end user.

保存条件 Store at -20 °C for one year. Avoid repeated freeze/thaw cycles. The lyophilized antibody is stable at room temperature for at least one month and for greater than a year when kept at -20°C. When reconstituted in sterile pH 7.4 0.01M PBS or diluent of antibody the antibody is stable for at least two weeks at 2-4 °C.

Important Note This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.

产品介绍 BEND2 is a 799 amino acid protein that contains two BEN domains. BEND2 exists as two alternatively spliced isoforms and is considered a complete proteome. BEN domain mediates protein–DNA and protein–protein interactions during chromatin organization and transcription. BEN domain may play a role in organization of viral DNA during replication or transcription. The BEND2 gene maps to human chromosome Xp22.13. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The X and Y chromosomes are the human sex BEND2蛋白抗体chromosomes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome.

Similarity : Contains 2 BEN domains.

Database links : UniProtKB/Swiss-Prot: Q8NDZ0.2