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McClung-Toabe Agar, Modified

[所屬分類:培養基配方] [發布時間:2021-12-1] [發布人:網站管理員2] [閱讀次數:] [返回]
McClung-Toabe Agar, Modified

山東拓普生物工程有限公司 培養基配方 //ljxinglong.com

Composition per liter:

Proteose peptone No. 2 .....................................40.0g
Agar ..................................................................20.0g
Na2HPO4 .............................................................5.0g
Glucose ...............................................................2.0g
NaCl....................................................................2.0g
KH2PO4...............................................................1.0g
MgSO4·7H2O ......................................................0.1g
Egg yolk emulsion, 50%............................. 100.0mL
Hemin solution................................................ 1.0mL
pH 7.6 ± 0.2 at 25°C
Egg Yolk Emulsion, 50%:
Composition per 100.0mL:
Chicken egg yolks..................................................11
Whole chicken egg...................................................1
NaCl (0.9% solution) .................................... 50.0mL
Preparation of Egg Yolk Emulsion, 50%:
Soak eggs with 1:100 dilution of saturated mercuric
chloride solution for 1 min. Crack eggs and separate
yolks from whites. Mix egg yolks with 1 chicken egg.
Measure 50.0mL of egg yolk emulsion and add to
50.0mL of 0.9% NaCl solution. Mix thoroughly. Fil
ter sterilize. Warm to 45°–50°C.
Hemin Solution:
Composition per 100.0mL:
Hemin..................................................................0.5g
NaOH (1N solution)...................................... 20.0mL
Preparation of Hemin Solution: Add hemin to
20.0mL of 1N NaOH solution. Mix thoroughly.
Bring volume to 100.0mL with distilled/deionized
water.
Preparation of Medium: Add components, ex
cept egg yolk emulsion, 50%, to distilled/deionized
water and bring volume to 900.0mL. Mix thoroughly.
Gently heat while stirring and bring to boiling. Auto
clave for 15 min at 15 psi pressure–121°C. Cool to
50°–55°C. Aseptically add 100.0mL of sterile egg
yolk emulsion, 50%. Mix thoroughly. Pour into ster
ile Petri dishes in 20.0mL volumes.
Use: For the cultivation of a wide variety of anaero
bic bacteria. For the differentiation of anaerobic bac
teria based on lecithinase production and lipase pro
duction. Bacteria that produce lecithinase appear as
colonies surrounded by a zone of insoluble precipi
tate. Bacteria that produce lipase appear as colonies
with a pearly iridescent sheen.
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