- 定做培养基/定制培养基
- 颗粒培养基
- 标准菌株生化鉴定试剂盒
- 预灌装即用型成品培养基
- 2025年版中国药典
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- 院感/疾控/体外诊断/采样管
- 样品采集与处理(均质)产品
- 按标准检索培养基
- 模拟灌装用培养基
- 干燥粉末培养基
- 培养基添加剂/补充剂
- 生化反应鉴定管
- 染色液等配套产品
- 对照培养基/标准品
- 实验耗材与器具
- 生化试剂/化学试剂
- 菌种鉴定服务
BHI with Glycerol and Reducing Agents (DSMZ Medium 215c)
山东拓普生物工程有限公司
Shandong Tuopu Biol-Engineering Co.,Ltd
BHI with Glycerol and Reducing Agents
(DSMZ Medium 215c)
培养基配方
Composition per liter:
Pancreatic digest of gelatin..................................14.5g
Brain heart, solids from infusion .............................6.0g
Peptic digest of animal tissue.................................6.0g
NaCl...........................................................5.0g
Glucose .......................................................3.0g
Na2HPO4 .......................................................2.5g
Glycerol solution............................................10.0mL
L- Cysteine·HCl–Na2S solution..............................10.0mL
pH 7.4 ± 0.2 at 25°C
Glycerol Solution:
Composition per 100.0mL:
Glycerol ....................................................87.0g
Preparation of Glycerol Solution: Add glycerol to distilled/de-
ionized water and bring volume to 100.0mL. Mix thoroughly.
L -Cysteine·HCl–Na2S Solution:
Composition per 100.0mL:
L- Cysteine·HCl.............................................2.5g
Na2S·9H2O...................................................2.5g
Preparation of L -Cysteine·HCl–Na2S Solution: Add L -
cysteine·HCl to distilled/deionized water and bring volume to 80.0mL.
Mix thoroughly. Adjust pH to 11 with NaOH. Add Na2S·9H2O. Mix
thoroughly. Bring volume to 100.0mL with distilled/deionized water.
Gently heat and bring to boiling under 100% N2 . Cool to 25°C under
100% N 2 . Autoclave for 15 min at 15 psi pressure–121°C.
Preparation of Medium: Add components, except L -cysteine·HCl–
Na2S solution, to distilled/deionized water and bring volume to 990.0mL.
Mix thoroughly. Gently heat and bring to boiling under 100% N2 . Cool to
25°C under 100% N2 . Autoclave for 15 min at 15 psi pressure–121°C.
Aseptically and anaerobically under 100% N2 add 10.0mL of L -
cysteine·HCl–Na2S solution. Mix thoroughly. Aseptically under 100% N2
distribute to tubes. Alternately distribute 10.0mL amounts of the medium
without L -cysteine·HCl–Na2S solution to tubes prior to autoclaving. Auto-
clave for 15 min at 15 psi pressure–121°C. Aseptically and anaerobically
add 1.0mL of L -cysteine·HCl–Na2S solution to each tube.
Use: For the cultivation of Clostridium sp.