021-51111890
购物车（）
sales@molnova.cn
CKS-17
CAS No. 99273-04-8
CKS-17 ( ——— )
产品货号. M41863 CAS No. 99273-04-8
CKS-17 是一种合成的逆转录病毒包膜肽。CKS-17 具有高度保守的氨基酸序列，出现在许多动物和人类逆转录病毒的跨膜包膜蛋白中。CKS-17 作为一种免疫调节表位，对许多免疫功能显示抑制特性。
纯度: >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| 规格 | 价格/人民币 | 库存 | 数量 |
| 25MG | 获取报价 | 有现货 |
|
| 50MG | 获取报价 | 有现货 |
|
| 100MG | 获取报价 | 有现货 |
|
| 500MG | 获取报价 | 有现货 |
|
| 1G | 获取报价 | 有现货 |
|
生物学信息
-
产品名称CKS-17
-
注意事项本公司产品仅用于科研实验，不得用于人体或动物的临床与诊断
-
产品简述CKS-17 是一种合成的逆转录病毒包膜肽。CKS-17 具有高度保守的氨基酸序列，出现在许多动物和人类逆转录病毒的跨膜包膜蛋白中。CKS-17 作为一种免疫调节表位，对许多免疫功能显示抑制特性。
-
产品描述CKS-17 is a synthetic retroviral envelope peptide. CKS-17 has the highly conserved amino acid sequences occurring within the transmembrane envelope protein of many animal and human retroviruses. CKS-17 acts as an immunomodulatory epitope and exhibits suppressive properties for numerous immune functions.
-
体外实验CKS-17 (10 μM; i.d.; B6AF1 mice and C57BL/6J mice) inhibits delayed-type hypersensitivity (DTH) reactions to sheep erythrocytes in the feet of mice.Animal Model:B6AF1 mice and C57BL/6J mice with DTH models Dosage:10 μM Administration: Intradermal injection, into the right hind footpad Result:Had a transient depressive effect on DTH reaction.
-
体内实验CKS-17 (THP-1 cells) induces increased intracellular cAMP via activation of adenylate cyclase.CKS-17 (15 μM; EL4 cells) inhibits interleukin-2 production by tumor cell products.
-
同义词———
-
通路Others
-
靶点Other Targets
-
受体———
-
研究领域———
-
适应症———
化学信息
-
CAS Number99273-04-8
-
分子量1942.31
-
分子式C87H148N26O24
-
纯度>98% (HPLC)
-
溶解度———
-
SMILES———
-
化学全称———
运输与储存
-
储存条件(-20℃)
-
运输条件With Ice Pack
-
稳定性≥ 2 years
参考文献
1. Haraguchi S, et, al. Induction of intracellular cAMP by a synthetic retroviral envelope peptide: a possible mechanism of immunopathogenesis in retroviral infections. Proc Natl Acad Sci U S A. 1995 Jun 6;92(12):5568-71.?
产品手册
关联产品
-
β-Lipotropin (1-10),...
β-Lipotropin (1-10), porcine
-
Wogonin 7-O-beta-D-g...
Wogonin 7-O-β-D-glucuronidemethylester 是从黄连解毒汤中分离出来的天然化合物。
-
4-CMTB
4-CMTB 是 FFA2 和 GPR43 的选择性激动剂。它也是正变构调节剂 (pEC50=6.38)。
