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Enteric Fermentation Base (Fermentation Base for Campylobacter)

[所属分类:培养基配方] [发布时间:2021-11-17] [发布人:网站管理员2] [阅读次数:] [返回]
Enteric Fermentation Base
(Fermentation Base for Campylobacter)

山东拓普生物工程有限公司 培养基配方 http://www.topbiol.com

Composition per liter:

Peptic digest of animal tissue ...........................10.0g
NaCl....................................................................5.0g
Beef extract.........................................................3.0g
Carbohydrate solution................................. 100.0mL
Andrade’s indicator....................................... 10.0mL
pH 7.2 ± 0.1 at 25°C
Source: This medium is available as a premixed
powder from BD Diagnostic Systems.
Carbohydrate Solution:
Composition per 100.0mL:
Carbohydrate.....................................................10.0g
Preparation of Carbohydrate Solution: Add
carbohydrate to distilled/deionized water and bring
volume to 100.0mL. Mix thoroughly. Filter sterilize.
Glucose, lactose, mannitol, sucrose, adonitol, arabi
nose, cellobiose, dulcitol, glycerol, inositol, salicin,
xylose, or other carbohydrates may be used. For the
preparation of expensive carbohydrate solutions
(adonitol, arabinose, cellobiose, dulcitol, glycerol,
inositol, salicin, or xylose), 5.0g of carbohydrate per
100.0mL of distilled/deionized water may be used.
Andrade’s Indicator:
Composition per 100.0mL:
NaOH (1N solution)...................................... 16.0mL
Acid Fuchsin.......................................................0.1g
Caution: Acid Fuchsin is a potential carcinogen
and care must be taken to avoid inhalation of the
powdered dye and contact with the skin.
Preparation of Andrade’s Indicator: Add
components to distilled/deionized water and bring
volume to 100.0mL. Mix thoroughly.
Preparation of Medium: Add components, ex
cept carbohydrate solution, to distilled/deionized wa
ter and bring volume to 900.0mL. Mix thoroughly.
Gently heat and bring to boiling. Distribute into tubes
that contain an inverted Durham tube in 9.0mL vol
umes. Autoclave for 15 min at 15 psi pressure–
121°C. Cool to 25°C. Aseptically add 1.0mL of ster
ile carbohydrate solution per tube. Mix thoroughly.
Use: For the cultivation and differentiation of a vari
ety of bacteria based on their ability to ferment differ
ent carbohydrates. Bacteria that produce acid from
carbohydrate fermentation turn the medium dark
pink to red. Bacteria that produce gas have a bubble
trapped in the Durham tube.
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