精品久久久久久,在线观看精品国产,久久不卡,久久就是精品,国产精品无码久久久久,亚洲日本一区二区三区高清在线,亚洲午夜精品一级在线

熱門搜索:A549    293T 金黃色葡萄球菌 大腸桿菌 AKK菌
購(gòu)物車 1 種商品 - 共0元
當(dāng)前位置: 首頁(yè) > ATCC代理 > Paramecium tetraurelia Sonneborn
最近瀏覽歷史
聯(lián)系我們
  • 0574-87157013
  • mingzhoubio@163.com
  • 浙江省寧波市鎮(zhèn)海區(qū)莊市街道興莊路9號(hào)
  • 創(chuàng)e慧谷42號(hào)樓B幢401室
Paramecium tetraurelia Sonneborn
Paramecium tetraurelia Sonneborn
規(guī)格:
貨期:
編號(hào):B221815
品牌:Mingzhoubio

標(biāo)準(zhǔn)菌株
定量菌液
DNA
RNA

規(guī)格:
凍干粉
斜面
甘油
平板


產(chǎn)品名稱 Paramecium tetraurelia Sonneborn
商品貨號(hào) B221815
Strain Designations stock 51.7K
Biosafety Level 1

Biosafety classification is based on U.S. Public Health Service Guidelines, it is the responsibility of the customer to ensure that their facilities comply with biosafety regulations for their own country.

Isolation
Spencer, IN, 1939
Product Format test tube
Type Strain no
Comments
Without Kappa.
Trichocyst phenotype transformation induced by macronuclear transplantation
Medium ATCC® Medium 802: Sonneborn's Paramecium medium
Growth Conditions
Temperature: 25.0°C
Protocol: ATCCNO: 30300 SPEC: This strain is shipped as a growing test tube culture. Upon arrival, remove test tube from sealed plastic envelope, remove plastic seal from cap, and loosen the cap one half turn. Add 1.0 ml of ATCC medium 802 bacterized with Enterobacter aerogenes ATCC 13048 twice weekly. When the tube is filled to within one inch of the top, decant leaving 5.0 ml in the original tube. Subcultures are established by transferring 0.5 ml of a growing culture to 5.0 ml of bacterized ATCC medium 802 in a 20 x 120 mm test tube.
Subcultivation
Protocol: ATCCNO: 30300 SPEC: This strain is shipped as a growing test tube culture. Upon arrival, remove test tube from sealed plastic envelope, remove plastic seal from cap, and loosen the cap one half turn. Add 1.0 ml of ATCC medium 802 bacterized with Enterobacter aerogenes ATCC 13048 twice weekly. When the tube is filled to within one inch of the top, decant leaving 5.0 ml in the original tube. Subcultures are established by transferring 0.5 ml of a growing culture to 5.0 ml of bacterized ATCC medium 802 in a 20 x 120 mm test tube.
Cryopreservation
Cryoprotective Solution

DMSO ?????????????????????????????????????????????????????????????????????????????????? 1.5 ml

Fresh growth medium w/o bacteria???????????????????????????????? 7.5 ml

MgCl2 (0.5 mM)??????????????????????????????????????????????????????????????????? 0.5 ml

CaCl2 (0.5 mM)??????????????????????????????????????????????????????????????????? 0.5 ml

1.???? Mix the components in the order listed.? Before adding the MgCl2 and the CaCl2 allow the solution to return to room temperature.? When the medium is added to the DMSO the solution will warm up due to chemical heat.

2. ??? Harvest cells from a culture that is at or near peak density by filtration and centrifugation at 200 x g for 1 min.

3.???? Adjust the concentration of cells at least 2 x 105/ml in fresh medium.

4.? ?? Mix the cell preparation and the cryoprotective solution in equal portions.

5.? ?? Dispense in 0.5 ml aliquots into 1.0 - 2.0 ml sterile plastic screw-capped cryules (special plastic vials for cryopreservation).

6. ??? Place vials in a controlled rate freezing unit. From room temperature cool at -1°C/min to -40°C. If freezing unit can compensate for the heat of fusion, maintain rate at -1°C/min through heat of fusion. At -40°C plunge ampules into liquid nitrogen.

7.? ?? Ampules are stored in either the vapor or liquid phase of a nitrogen refrigerator.

8.? ?? To establish a culture from the frozen state add 1.0 ml bacterized ATCC medium 802 to the frozen ampule and place it in a 35°C water bath.? Immerse the vial to a level just above the surface of the frozen material. Do not agitate the vial.

9.???? Immediately after thawing, do not leave in water bath, aseptically remove the contents of the ampule and inoculate onto the surface of an ATCC medium 919 (non-nutrient agar) plate containing an overlay of 15.0 ml of bacterized ATCC medium 802.

10.? Incubate at 25°C with the cap on loosely.

11.? Once the culture is established, transfer 0.5 ml to 5.0 ml of bacterized ATCC medium 802.

12.? Follow the protocol for maintenance of culture.

Name of Depositor TM Sonneborn
Chain of Custody
ATCC <<--TM Sonneborn<<--. . . <<--- M. Clemmer
Year of Origin 1939
References

Aufderheide KJ. Trichocyst phenotype transformation induced by macronuclear transplantation in Paramecium tetraurelia. Exp. Cell Res. 156: 282-286, 1985. PubMed: 3965292

梅經(jīng)理 17280875617 1438578920
胡經(jīng)理 13345964880 2438244627
周經(jīng)理 17757487661 1296385441
于經(jīng)理 18067160830 2088210172
沈經(jīng)理 19548299266 2662369050
李經(jīng)理 13626845108 972239479
绍兴市| 高安市| 蒲城县| 都兰县| 海淀区| 昌乐县| 广西| 安泽县| 萨嘎县| 襄汾县| 神木县| 平果县| 正安县| 寿阳县| 新龙县| 朝阳县| 保靖县| 航空| 韶关市| 西乌珠穆沁旗| 郎溪县| 淳化县| 平和县| 拉孜县| 福建省| 土默特左旗| 日喀则市| 平阳县| 名山县| 开封市| 昌都县| 普格县| 蚌埠市| 民勤县| 禄丰县| 南木林县| 苏尼特右旗| 墨玉县| 庄浪县| 珠海市| 平武县|