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上海科敏生物科技有限公司
货号:P0143
规格:肠杆菌科细菌的生化试验
包装:250克
保存条件:RT
CAS:/三糖铁琼脂培养基/三糖铁培养基/TSI琼脂/Triple Sugar Iron Agar相关产品>>>>
Z0037 CAS:76738-62-0/多效唑/1-对氯苯基-2-(1,2,4-三唑-1-基)-4,4-二甲-3-戊醇/(2RS,3RS)-1-(4-氯苯基)-4,4-二甲基-2-(1H-1,2,4-三唑-1-基)戊-3-醇/氯丁唑/1-(4-氯苯基)-4,4-二甲基-2-(1,2,4-三唑-1-基)-3-戊醇/Paclobutrazol/PP333
T0169 CAS:69227-93-6/十二烷基-β-D-麦芽糖苷/月桂酰基麦芽糖苷/N-十二烷基-β-D-麦芽苷/N-十二烷基-β-D-麦芽糖/DDM
P0235 CAS:/抗生素Ⅵ号培养基/抗生素6号培养基/Antibiotic Agar NO.6
Z0037 CAS:76738-62-0/多效唑/1-对氯苯基-2-(1,2,4-三唑-1-基)-4,4-二甲-3-戊醇/(2RS,3RS)-1-(4-氯苯基)-4,4-二甲基-2-(1H-1,2,4-三唑-1-基)戊-3-醇/氯丁唑/1-(4-氯苯基)-4,4-二甲基-2-(1,2,4-三唑-1-基)-3-戊醇/Paclobutrazol/PP333
Q1043 CAS:10101-41-4/硫酸钙/生石膏/石膏/二水合硫酸钙/白土/纯白生石膏/白色软粘土/制管土/石膏粉/纤维石/雪花石膏/透石膏/Calcium sulfate dihydrate
P0068 CAS:/血粉蛋白胨
A0198 CAS:65094-46-0/甘氨酰-脯氨酰-对硝基苯胺对甲苯磺酸盐/GPDA
D0025 CAS:9007-83-4/γ-球蛋白(牛)/牛丙种球蛋白/普通丙种球蛋白/γ-Globulins from bovine blood
P0416 CAS:/SIM动力培养基/SIM培养基/Motility Test Medium(Semisolid)
P0618 CAS:/山梨酸发酵管
C0034 CAS:/一氧化氮合成酶测试盒[测总NOS(T-NOS)]/NOS测试盒[测总NOS(T-NOS)]
Q0556 CAS:142-08-5/2-羟基吡啶/2-吡啶酚/2-吡啶酮/2-Hydroxypyridine
S0242 CAS:804-63-7/硫酸奎宁/(8S,9R)-6'-甲氧基金鸡纳-9-醇硫酸盐/奎宁硫酸盐/奎宁硫酸酯/硫酸喹啉/硫酸金鸡纳盐/Quinine sulfate
Q0768 CAS:12007-58-8/硼酸铵/硼酸氢铵/偏硼酸铵/四硼酸铵/Ammonium borate
Z0148 CAS:/花宝3号/N-P-K
P0455 CAS:/酪蛋白琼脂/水解酪蛋白琼脂/Casein Agar Medium
P0469 CAS:/LIM培养基/赖氨酸吲哚动力培养基/赖氨酸靛基质动力培养基/LIM Medium
S0055 CAS:62698-55-9/百里酚酞络合指示剂/百里香酚酞络合指示剂/麝香草酚酞络合指示剂/百里酚酞氨羧络合剂/麝香草酚酞钠络合剂/TPC
Q0953 CAS:298-14-6/碳酸氢钾/重碳酸钾/酸性碳酸钾/酸式碳酸钾/K-Lyte
F0116 CAS:9004-54-0/葡聚糖T2000/葡聚糖D2000/右旋糖酐2000/Dextran T2000
CAS:/三糖铁琼脂培养基/三糖铁培养基/TSI琼脂/Triple Sugar Iron Agar关键词:CAS:/三糖铁琼脂培养基/三糖铁培养基/TSI琼脂/Triple Sugar Iron Agar
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文献和实验. Glycation of proteins by reducing sugars (Maillard reaction) results in a profile of time-dependent adduct evolution rendering susceptibility to oxidative elaboration. In addition, oxidative stress can result in oxidized sugar derivatives
to mix together and then add to agar to make plates. Making amino acid dropout (CSM) solution Generally easiest to make a 10x master solution that you can dilute back when you''re pouring plates. Let''s assume you''re going to make 200ml
, this method for preparing competent E. coli from Inoue et al. (1990) can challenge the efficiencies achieved by Hanahan (1983). However, under standard laboratory conditions, efficiencies of 1 x 108 to 3 x 108 transformed colonies/mg of plasmid DNA
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