北京百歐博偉生物談談 亞硝化單胞菌 ATCC BAA-120的培養(yǎng)注意事項
Nitrosomonas europaea Winogradsky 菌株拉丁名
(ATCC? BAA-1201?) 菌株編號
Strain Designations菌株別名: ML1 /
Type Strain 模式菌株: no /
Biosafety Level 生物安全等級 : 1
Strain Designations 菌株別名 ML1
Isolation 分離源 Sludge Wisconsin, United States isolation date: September, 2003
Type Strain 模式菌株no
Biosafety Level 生物安全等級 1
Product Format 提供形式 frozen
Medium 培養(yǎng)基 ATCC? Medium 2265: Nitrosomonas europaea medium
Growth Conditions 生長條件
Temperature 培養(yǎng)溫度 : 30.0℃
Name of Depositor 寄存人 DR Noguera, H Park Special Collection NSF - Bacteriology
Isolation Sludge Wisconsin, United States
isolation date: September, 2003
Year of Origin 收藏年份 2003
References 參考文獻 Park HD, Noguera DR. Evaluating the effect of dissolved oxygen on ammonia-oxidizing bacterial communities in activated sludge.. Water Res. 38: 3275-3286, 2004. PubMed: 15276744
chemostat reactor seeded with activated sludge, Marshall wastewater treatment plant, Marshall, WI
其中開通海外直郵業(yè)務專業(yè)代理美國ATCC微生物菌種保藏中心菌種細菌和噬菌體(18380)細胞系和雜交瘤(5004);真菌和酵母(58208)
原代細胞(143);原生動物和藻類(2426)
干細胞(102);載體,克隆與分子(18005);病毒(3598)除了專利和受控產品其他均可供應,全方位滿足您實驗需求,另到貨時間短COA齊全。
Medium 培養(yǎng)基 ATCC? Medium 18: Trypticase Soy Agar/Broth
那么培養(yǎng)時間應該注意什么呢?
Propagation Procedure
1.Open vial according to enclosed instructions.
2.From a single tube of #18 broth (5 to 6 ml), withdraw approximately 0.5 to 1.0 ml with a Pasteur or 1.0 ml pipette and use to rehydrate the entire pellet.
3.Use 0.1 ml of this suspension to inoculate #18 slants and 0.1ml to inoculate #18 plates.
4.Incubate tubes and plates at 30oC, under aerobic conditions, for 24 hours.
5.After 24 hours of incubation, wash cells from the slant and transfer this broth to a new slant and plate. Incubate another 24 hours under aerobic conditions. This second transfer and incubation is necessary for complete removal of the cryoprotectant, which can inhibit growth.
1.根據(jù)隨附的說明打開樣品瓶。
2.從#18肉湯(5至6毫升)的單管中,用巴斯德或1.0毫升移液管取出約0.5至1.0毫升,并用于再水化整個顆粒。
3.使用0.1ml該懸浮液接種#18斜面和0.1ml接種#18板。
4.在有氧條件下,在30℃下孵育管和板24小時。
5.孵育24小時后,從斜面洗滌細胞并將該肉湯轉移到新的斜面和平板上。 在有氧條件下再孵育24小時。 這種第二次轉移和溫育對于完全除去可以抑制生長的冷凍保護劑是必需的。