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- 详细信息
- 文献和实验
- 技术资料
- 保存条件:
低温运输、-20℃保存,
- 保质期:
6个月
- 英文名:
Amphotericin B Solution
- 库存:
大量
- 供应商:
上海钰博生物科技有限公司
- 规格:
1 mL/盒
产品及特点
两性霉素B(二性霉素B;节丝霉素B;Fungizone)分子式:C47H73NO17,分子量:924.08,CAS号:1397-89-3,可溶性两性霉素B系来自链霉菌的多烯抗真菌类抗生素,它与真菌细胞膜的固醇类物质,特别是麦角固醇有亲和性,在膜上形成通道,使一些小分子流失。抗菌谱为真菌和酵母,多用于细胞培养。在日光下易被破坏失效。本品为浓度为20mg/mL的水溶液。
可溶性两性霉素B溶液,20mg/mL-Amphotericin B Solution低温运输、-20℃避光保存,有效期6个月。D2087-00 HP Plant DNA Maxi Kit(2)
D2087-01 HP Plant DNA Maxi Kit(5)
D2087-02 HP Plant DNA Maxi Kit(20)
磁珠植物DNA提取试剂盒:从小于100mg植物组织中提取高分子量基因组DNA
M2327-01 Mag-Bind Plant DNA Kit(50)
M2327-02 Mag-Bind Plant DNA Kit(200)
磁珠植物DNA大量提取试剂盒:从植物组织中纯化高达2.5mg高纯度的基因组DNA
M2588-01 Mag-Bind Plant DNA Maxi Kit(10)
M2588-02 Mag-Bind Plant DNA Maxi Kit(50)
96孔磁珠植物DNA提取试剂盒:从小于100mg植物组织提取高分子量DNA
M1027-01 Mag-Bind Plant DNA Kit(2x96)
M1027-02 Mag-Bind Plant DNA Kit(8x96)
真菌DNA抽提试剂盒
真菌DNA小量提取试剂盒:从100mg真菌组织或细胞中提取基因组DNA
D3390-00 Fungal DNA Kit(5)
D3390-01 Fungal DNA Kit(50)
D3390-02 Fungal DNA Kit(200)
D1090-01 E-Z 96 Fungal DNA Kit(2x96)
D1090-02 E-Z 96 Fungal DNA Kit(8x96)
真菌DNA中量提取试剂盒:从500mg新鲜真菌组织或150mg干燥真菌组织提取基因组DNA
D3590-01 Fungal DNA Midi Kit(10)
D3590-02 Fungal DNA Midi Kit(25)
真菌DNA大量提取试剂盒:从1g真菌组织样品中提取基因组DNA
D3690-01 Fungal DNA Maxi Kit(5)
D3690-02 Fungal DNA Maxi Kit(20)
SP真菌DNA小量提取试剂盒:从真菌组织或细胞中提取基因组DNA
D5542-00 SP Fungal DNA Kit(5)
D5542-01 SP Fungal DNA Kit(50)
D5542-02 SP Fungal DNA Kit(200)
SP真菌DNA中量提取试剂盒:从真菌组织或细胞中提取基因组DNA
D5545-00 Sp Fungal DNA Midi Kit(2)
D5545-01 Sp Fungal DNA Midi Kit(10)
D5545-02 Sp Fungal DNA Midi Kit(25)
HP真菌DNA小量抽提试剂盒
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文献和实验b-galactosidase Solution Assay
.1 g up to 500 ml 50 mM CPRG 0.0304 g chlorophenyl red b-galactopyranoside (Boehringer Mannheim #834-308) up to 1 ml with Q store in the dark at -20° Procedure • Wash cells or tissue twice in PBS, pellet and resuspend in 150 microliters
b-galactosidase Solution Assay
b-galactosidase Solution Assay Reference: Simon and Lis (1987) NAR 15 : 2971-2988. Solutions CPRG Assay Buffer 50 mM KPO4 pH 7.5 5 ml 1M KPO4 pH 7.5 1 mM MgCl2 0.1 ml 1M MgCl 2 up to 100 ml with Q
Azatides as Peptidomimetics: Solution and Liquid Phase Syntheses
(3 ), substitutions (1a ,b ), and most recently backbone modifications (4 ). It is this latter development that has been exploited for the synthesis of biomimetic polymeric structures. Such progress has been fueled by the suggestion that peptidomimetics may provide
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