KSPWFTTL TFA

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KSPWFTTL TFA  纯度: 99.16%

KSPWFTTL TFA 是一种来自 p15E 跨膜蛋白的免疫显性 Kb 限制性表位。KSPWFTTL TFA 可以恢复肿瘤系对抗 AKR/Gross MuLV 细胞毒性 T 淋巴细胞的敏感性。

KSPWFTTL TFA

KSPWFTTL TFA Chemical Structure

规格 价格 是否有货 数量
5 mg ¥3000 In-stock
10 mg ¥4800 In-stock
50 mg   询价  
100 mg   询价  

* Please select Quantity before adding items.

KSPWFTTL TFA 相关产品

相关化合物库:

  • Bioactive Compound Library Plus
  • Immunology/Inflammation Compound Library
  • Anti-Cancer Compound Library
  • Peptide Library

生物活性

KSPWFTTL TFA is an immunodominant Kb-restricted epitope from the p15E transmembrane protein. KSPWFTTL TFA can restore susceptibility of a tumor line to anti-AKR/Gross MuLV cytotoxic T lymphocytes[1][2].

体外研究
(In Vitro)

KSPWFTTL TFA is derived from the retroviral p15 TM envelope protein. The cytolytic T-lymphocyte (CTL)-insusceptible, variant cl.18-5 clonal line, after pulsed with the KSPWFTTL TFA peptide, becomes susceptible to lysis by antiviral CTL[2].

上海金畔生物科技有限公司 has not independently confirmed the accuracy of these methods. They are for reference only.

分子量

1093.15

Formula

C50H71F3N10O14

Sequence

Lys-Ser-Pro-Trp-Phe-Thr-Thr-Leu

Sequence Shortening

KSPWFTTL

运输条件

Room temperature in continental US; may vary elsewhere.

储存方式

Sealed storage, away from moisture

Powder -80°C 2 years
-20°C 1 year

*In solvent : -80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)

溶解性数据
In Vitro: 

H2O : 66.67 mg/mL (60.99 mM; Need ultrasonic)

配制储备液
浓度 溶剂体积 质量 1 mg 5 mg 10 mg
1 mM 0.9148 mL 4.5739 mL 9.1479 mL
5 mM 0.1830 mL 0.9148 mL 1.8296 mL
10 mM 0.0915 mL 0.4574 mL 0.9148 mL

*

请根据产品在不同溶剂中的溶解度选择合适的溶剂配制储备液;一旦配成溶液,请分装保存,避免反复冻融造成的产品失效
储备液的保存方式和期限:-80°C, 6 months; -20°C, 1 month (sealed storage, away from moisture)。-80°C 储存时,请在 6 个月内使用,-20°C 储存时,请在 1 个月内使用。

参考文献
  • [1]. White HD, et, al. An immunodominant Kb-restricted peptide from the p15E transmembrane protein of endogenous ecotropic murine leukemia virus (MuLV) AKR623 that restores susceptibility of a tumor line to anti-AKR/Gross MuLV cytotoxic T lymphocytes. J Virol. 1994 Feb;68(2):897-904.

    [2]. Rich RF, et, al. Antiretroviral cytolytic T-lymphocyte nonresponsiveness: FasL/Fas-mediated inhibition of CD4(+) and CD8(+) antiviral T cells by viral antigen-positive veto cells. J Virol. 1999 May;73(5):3826-34.

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