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| 规格: | 1mg | 产品价格: | ¥268.0 |
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| 规格: | 5mg | 产品价格: | ¥473.0 |
| 规格: | 10mg | 产品价格: | ¥701.0 |
| 规格: | 25mg | 产品价格: | ¥1132.0 |
| 规格: | 50mg | 产品价格: | ¥1546.0 |
| 规格: | 100mg | 产品价格: | ¥2070.0 |
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Product Introduction
Bioactivity
| 名称 | Peptide T acetate(106362-32-7 free base) |
| 描述 | Peptide T acetate is an octapeptide from the V2 region of HIV-1 gp120. Peptide T is a synthetic octapeptide whose possible mechanism of action is the competitive inhibition of gp120 to the CD4 receptor as well as binding to vasointestinal peptide receptors and inhibiting cytokine action |
| 体外活性 | Peptide T通过抑制MAGI细胞测定中的病毒进入并在使用ADA外壳伪装的HIV病毒颗粒的荧光素酶报告测定中阻断感染来发挥作用。Peptide T选择性地通过趋化因子受体CCR5而非CXC4抑制HIV复制[2]。在10^-8 M浓度下,Peptide T诱导人类Th2细胞系和PBMC产生IL-10。同样,在10^-9 M浓度下,Peptide T显著抑制PBMC产生IFN-g[3]。 |
| 体内活性 | Peptide T通过皮下注射的方式,在实验性自身免疫性脑脊髓炎(EAE)病程的不同阶段和剂量进行给药,然而,Peptide T既不能预防也不能改善EAE[4]的病情。 |
| 存储条件 | Keep away from moisture Powder: -20°C for 3 years | In solvent: -80°C for 1 year Shipping with blue ice/Shipping at ambient temperature. |
| 溶解度 | H2O : 5 mM, Sonication is recommended. DMSO : Insoluble |
| 关键字 | Peptide T acetate(106362-32-7 free base) | Peptide T acetate(106362327 free base) | Peptide T acetate(106362 32 7 free base) | HIVProtease | HIV-1 | HIV Protease | CD4 |
| 相关产品 | Tenofovir | Valproic Acid | Chloroquine phosphate | (-)-Epigallocatechin Gallate | Emtricitabine | Dolutegravir intermediate-1 | Dextran sulfate sodium salt (MW 5000) | Lamivudine | 5-Fluorouracil | Decanedioic acid | Stavudine | Dimethyl fumarate |
| 相关库 | Inhibitor Library | Bioactive Compound Library | Bioactive Compounds Library Max | Anti-Infection Compound Library | Peptide Compound Library | NO PAINS Compound Library | Anti-Viral Compound Library |
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文献和实验Two dimensional peptide mapping
This specfic protocol is the latest incarnation of peptide mapping procedures that have been developed here in the TVL/MBVL of the Salk Institute over the last 20 years. Wade Gibson developed the first peptide mapping protocol
Synthetic Peptide Libraries for T-Cell Epitope Identification
This chapter describes a methodology for elucidating immunogenic epitopes stimulatory for CD4 + T-cell clones (Fig. 1 ). The methodology makes use of synthetic peptide libraries and must be regarded as an alternative
Metabolic Engineering for Acetate Control in Large Scale Fermentation
oxidase (poxB ) and over-expression of acety-CoA synthetase (acs ) in E. coli K strain for controlling acetate accumulation. A recombinant peptide was expressed and produced in the engineered strains with a very low acetate �formation in a 10-L
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