ATCCPRA-302 WA1 ATCC細(xì)胞代理
- 公司名稱 北京北納創(chuàng)聯(lián)生物技術(shù)研究院
- 品牌
- 型號(hào) ATCCPRA-302
- 產(chǎn)地 美國(guó)
- 廠商性質(zhì) 生產(chǎn)廠家
- 更新時(shí)間 2024/11/9 20:59:30
- 訪問次數(shù) 1823
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北京標(biāo)準(zhǔn)物質(zhì)網(wǎng)隸屬于北京北納創(chuàng)聯(lián)生物技術(shù)研究院,，具備強(qiáng)大的分析測(cè)試,、技術(shù)開發(fā)、*,、物流管理和售后服務(wù)能力,，并與國(guó)內(nèi)外眾多檢測(cè)機(jī)構(gòu)、科研院校和工廠企業(yè)有著良好和穩(wěn)定的合作關(guān)系,，具有較強(qiáng)的性和影響力,。
北納生物也隸屬于北京北納創(chuàng)聯(lián)生物技術(shù)研究院，實(shí)驗(yàn)基地總占地面積16畝,，并設(shè)有細(xì)胞庫(kù),、微生物菌種保藏庫(kù)，細(xì)胞培養(yǎng),、菌種培養(yǎng)等實(shí)驗(yàn)室,。擁有細(xì)胞和菌株2萬(wàn)余株，并設(shè)有生物資源信息庫(kù),，收錄信息達(dá)20余萬(wàn)株,。致力于提供實(shí)驗(yàn)室綜合解決方案，為廣大客戶服務(wù),。
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ATCCPRA-302 WA1 ATCC細(xì)胞代理
| 基本信息 | |
| 資源編號(hào) | ATCCPRA-302 |
| 資源名稱 | WA1 |
| 種屬 | Babesia duncani |
| 分離基物 | Human blood, Washington State, 1991 |
| 提供形式 | frozen |
| 安全等級(jí) | 2 |
| 模式菌株 | no |
| 應(yīng)用領(lǐng)域 | Vector borne research |
| 培養(yǎng)方法 | |
| 生長(zhǎng)條件 | Temperature: 25°C Culture System: in vivo c*tion, hamster |
| 存儲(chǔ)條件 | Frozen Cultures:-70°C for 1 week; liquid N2 vapor for long term storageFreeze-dried Cultures:2-8°CLive Cultures:See Protocols section for handling information;Reagents Alsever's Solution NaCl, 4.2 g Na3citrate·2H2O, 8.0 g Glucose, 20.5 g Glass distilled H2O to 1.0 L *Dissolve components in glass distilled H2O, adjust the pH to 6.1 with 10% (w/v) citric acid and filter sterilize. The solution can be obtained from Sigma-Aldrich (cat# A3551). Harvest and Preservation Prepare a 30% (v/v) sterile glycerol solution in Alsever's solution. Draw approximately 0.5 mL of anticoagulant solution (Yaeger's or heparin, etc.) into a syringe and move it back and forth over the length of the syringe, several times. Remove all air bubbles. Draw blood by cardiac puncture into the syringe from a host animal that has reached or is near peak parasitemia. If clotting occurs during extraction of blood, insufficient heparin was used. Mix the heparinized blood with the 30% glycerol solution in a 2:1 ratio. If any clotting has occurred do not use. After mixing, the final concentration of cryoprotectant solution will be 10% (v/v). The mixture should be placed in a 4°C ice bath. The time from the mixing of the cell preparation and glycerol stock solution before the freezing process is begun should be no less than 15 min and no longer than 30 min. Dispense in 0.5 mL aliquots into 1.0 mL to 2.0 mL sterile plastic screw-capped cryules (special plastic vials for cryopreservation). Filled ampules should be placed in a 4°C ice bath. Do not immerse ampules to the level of the vial cap. Plunge ampules from 4°C into liquid nitrogen. The frozen preparations may be stored in a mechanical freezer until needed, however storage in either the vapor or liquid phase of a nitrogen refrigerator is recommended for the longest viability. To thaw a frozen ampule, place in a 35°C water bath, until thawed (2 to 3 min). Immerse the ampule just sufficient to cover the frozen material. Do not agitate the ampule. Immediately after thawing, aseptically remove the contents of the ampule with a syringe and inoculate an uninfected hamster. Follow the protocol for maintenance in vivo. The course of infection may be longer or shorter than usual depending on percent recovery of the parasite from the frozen state. |
| 詳細(xì)說明 | |
| 描述 | Strain has been passaged in vivo in jirds several times |
| Year of Origin | 1991 |
ATCCPRA-302 WA1 ATCC細(xì)胞代理
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