Human NPC2 Protein C-His Tag | Syd Labs BP003237
(悉得)Syd Labs 货号:BP003237 Human NPC2 Protein with the C-His Tag (人 NPC2 蛋白 C-His 标签) is expressed from HEK293 with His tag at the C-terminal.It contains Glu20-Leu151.
产品参数
| 货号 | BP003237 |
|---|---|
| 产品名称 | Human NPC2 Protein C-His Tag | Syd Labs BP003237 |
| 供货商名称 | Syd Labs, Inc. |
| 品牌名 | Syd Labs |
| 物种 | Human |
| 来源 | The recombinant Human NPC2 Protein, (amino acids Glu20-Leu151) fused with a His tag at the C-terminus, was produced in HEK 293 cells. |
| Accession | P61916-1 |
| 产品标签 | C-His |
| 生物素化 | no |
| 确定序列 | Glu20-Leu151 |
| 分子量 | The recombinant Human NPC2 protein with the His tag at the C-terminus has a predicted MW of 15.67 kDa. Due to glycosylation, the protein migrates to 21-24 kDa and 27-35 kDa kDa based on Tris-Bis PAGE result. |
| Form | Liquid |
| 形式 | Supplied as 0.22μm filtered solution in PBS (pH 7.4). |
| 制剂 | It is recommended to reconstitute the lyophilized recombinant Human NPC2 Protein in sterile H2O to a protein concentration not less than 100 ug/ml. Centrifuge the tube before opening. |
| 纯度 | >95% by SEC-HPLC and SDS-PAGE under reducing conditions. |
| 内毒素 | Less than 1 EU per ug of protein as determined by LAL method. |
| 运输 | The recombinant Human NPC2 Protein is shipped with ice pack. Upon receipt, store it immediately at the temperature recommended below. |
| 稳定性与储存 | Valid for 12 months from date of receipt when stored at -80°C.;Recommend to aliquot the protein into smaller quantities for optimal storage. Please minimize freeze-thaw cycles. |
| 注意事项 | Conditions of optimal recombinant Human NPC2 Protein performance should be determined experimentally by the investigator. |
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文献
BP003237: Human NPC2 Protein with the C-His Tag (人 NPC2 蛋白 C-His 标签)
The Niemann Pick type C (NPC) proteins, NPC1 and NPC2, are involved in the lysosomal storage disease, NPC disease. The formation of a NPC1⁻NPC2 protein⁻protein complex is believed to be necessary for the transfer of cholesterol and lipids out of the late endosomal (LE)/lysosomal (Lys) compartments. Mutations in either NPC1 or NPC2 can lead to an accumulation of cholesterol and lipids in the LE/Lys, the primary phenotype of the NPC disease.
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