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Claudin-9 Protein, Human, Recombinant

产品编号 TMPY-06902

Claudin-9 Protein, Human, Recombinant is expressed in HEK293 mammalian cells. The predicted molecular weight is 22.9 kDa and the accession number is O95484.

Claudin-9 Protein, Human, Recombinant

Claudin-9 Protein, Human, Recombinant

产品编号 TMPY-06902
Claudin-9 Protein, Human, Recombinant is expressed in HEK293 mammalian cells. The predicted molecular weight is 22.9 kDa and the accession number is O95484.
规格价格库存数量
20 μg¥ 6,3905日内发货
100 μg¥ 13,4005日内发货
500 μg¥ 47,4005日内发货
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产品信息

生物活性
Immobilized Human CLDN9-VLP (Full Length) Protein at 5 μg/mL (100 μL/well) can bind Anti-Human CLDN9 Antibody,Human IgG1, the EC50 is 1-10 ng/mL.
产品描述
Claudin-9 Protein, Human, Recombinant is expressed in HEK293 mammalian cells. The predicted molecular weight is 22.9 kDa and the accession number is O95484.
种属
Human
表达系统
HEK293 Cells
标签Tag Free
蛋白编号O95484
蛋白构建
A DNA sequence encoding the human CLDN9 (O95484) (Met1-Val217) was expressed. Predicted N terminal: Met 1
分子量22.9 kDa (predicted)
内毒素< 1.0 EU/μg of the protein as determined by the LAL method.
缓冲液Supplied as sterile 50 mM Hepes, 150 mM NaCl, 10% Trehalose, pH 7.2.
复溶方法
A Certificate of Analysis (CoA) containing reconstitution instructions is included with the products. Please refer to the CoA for detailed information.
存储
It is recommended to store the product under sterile conditions at -20°C to -80°C. Samples are stable for up to 12 months. Please avoid multiple freeze-thaw cycles and store products in aliquots.
运输方式In general, Lyophilized powders are shipping with blue ice. Solutions are shipping with dry ice.
研究背景
Claudin-9 (CLDN9) belongs to the claudins family and is a transmembrane protein found in tight junctions with two extracellular loops and a cytoplasmic C tail. CLDN9 modulates the ion- and charge-specific permeability of the paracellular pathway in most epithelial tissues. It forms heterotypic interactions with other claudins to create cation-selective channels in the kidney and may contribute to the maintenance of alveolar barrier function in the lung. Deficiency is shown to be associated with autosomal recessive deafness, DFNB116. CLDN9 expression has been shown to be upregulated in certain types of cancer, such as endometrial cancer and hepatocellular carcinoma, and its knockdown has been found to reduce cell proliferation and migration in vitro.

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