Recombinant Human CD264/TNFRSF10D Protein, C-hFc and His tag
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产品编号
KMH413
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别名
肿瘤坏死因子受体超家族成员10D, DCR2, CD264, TRUNDD, TRAILR4, TRAIL R4, TNF receptor superfamily member 10d
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规格
- 20ug
 - 50ug
 - 100ug
 - 200ug
 - 1mg
 
 
| Catalog Number | KMH413 | 
| Alias | 肿瘤坏死因子受体超家族成员10D, DCR2, CD264, TRUNDD, TRAILR4, TRAIL R4, TNF receptor superfamily member 10d | 
| Size | 20ug, 50ug, 100ug, 200ug, 1mg | 
| Product Description | KMH413 Recombinant Human CD264/TNFRSF10D Protein, C-hFc and His tag contains the human TNFRSF10D(56-211 aa) was expressed in Mammalian cells. | 
| Molecular Name | TNFRSF10D | 
| Product Introduction | TNFRSF10D参与细胞凋亡的调节和免疫应答的启动。 | 
| Molecular Weight | 60-70kD | 
| Expression System | HEK293F Cells | 
| Species | Human | 
| Concentration | 联系销售经理获得最新批次的浓度 | 
| Purity | ≥95% | 
| SDS-PAGE | ![]()  | 
| Purification | Affinity Purification | 
| Uniprot ID | Q9UBN6 | 
| Storage Condition | Store the product under sterile conditions after opening at -80℃ for 12 months. Store the lyophilized powder at -20℃. Avoid repeated freeze-thaw cycles. | 
| Formulation | PBS | 
| Shipping Condition | This product is shipped on ice packs or dry ice. | 
| Background | TNF-related apoptosis-inducing ligand receptor 4 (TRAIL R4) is a decoy receptor that negatively regulate TRAIL-induced cytotoxicity by competing for ligand binding with TRAIL-R1 and TRAIL-R2.1 TRAIL R4 is expressed mainly on CD8+ and NK cells and induces apoptosis in many tumour cells, but not in normal cells. TRAIL-R4 contains partially truncated death domain and therefore is unable to induce apoptosis and serves as a negative regulator of apoptotic signaling by impairment death-inducing signaling complex (DISC) processing. | 
| Endotoxin | < 0.1 EU per ug | 
| Protein Family | CD molecule | 
| Biological Activity | Measured by its ability to inhibit TRAILmediated cytotoxicity using L-929 mouse fibroblast cells treated with TRAIL. The ED50 for this effect is 1.8-7.2 ng/mL in the presence of 20 ng/mL | 
| Product Declaration | 该产品仅供科研使用,不可直接用于人体或注射。 | 
可以使用ELISA、Western blot或免疫沉淀等技术来检测蛋白与特定抗体的结合反应性。
使用温和的纯化条件、优化缓冲液成分和减少操作步骤,可以有效减少蛋白的损失。
							
							
							
							
						
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