TB1感受态细胞

库存 ：41

英文名 ：TB1 Chemically Competent Cell

保质期 ：12个月

供应商 ：江西江蓝纯生物试剂有限公司

保存条件 ：避光保存

规格 ：10×100ul/50×100ul

TB1感受态细胞

TB1 Chemically Competent Cell

产品货号： JLC-G025  
                     
保存条件： -80℃   

产品规格：10×100μl  50×100μl

产品介绍：
 
基因型 : 
F– ara Δ(lac-proAB) rpsL (Strr)[φ80 dlacΔ(lacZ)M15] thi hsdR

简单说明 : 
TB1感受态细胞来源于JM 83，是JM 83 hsdR型，只含有大肠杆菌RNA polymerase，缺少 BL21 (DE3)菌株的 T7 RNA polymerase，适合NEB公司的pMAL 系列质粒原核蛋白表达(The pMAL  vectors use the E. coli RNA polymerase)，不能用于pET系列质粒的表达，具有链霉素抗性。 High5TM系列TB1感受态细胞由特殊工艺制作，经pUC19质粒检测转化效率高达108cfu/μg。

操作说明 : 
1. 取100μl冰上融化的TB1感受态细胞，加入目的质粒并轻轻混匀，冰上静置25分钟。

2. 42℃水浴热激45秒，迅速放回冰上并静置2分钟，晃动会降低转化效率。

3. 向离心管中加入700μl不含抗生素的无菌培养基(2YT或LB)，混匀后37℃，200rpm复苏60分钟。

4. 5000rpm离心一分钟收菌，留取100μl左右上清轻轻吹打重悬菌块并涂布到含相应抗生素的2YT或LB培养基上。

5. 将平板倒置放于37℃培养箱过夜培养。

注意事项 :
1. 感受态细胞在冰上融化。

2. 混入质粒时应轻柔操作。

3. 转化高浓度的质粒可相应减少终用于涂板的菌量。

4. 诱导时，IPTG浓度可选(0.1-2mM均可)。

5. 为获得需要量的蛋白，佳诱导时间，温度，IPTG浓度需实验者优化。

Sample Induction Protocol (for reference only)
1.   Inoculate a single colony from a freshly streaked plate into 3ml of LB medium containing the appropriate antibiotic for the plasmid and host strain.
2.   Incubate with shaking at 200 rpm at 37℃ overnight. 
3.   Inoculate 50 ml of LB medium containing the appropriate antibiotic with 0.5 ml of the overnight culture prepared in step 2(use the 500 ml triangular flask as the container would be better).
4.   Incubate with shaking at 150 rpm at 37℃ until the OD 600 reaches 0.5-0.8. (0.6 recommended; about 2.5h).
5.   (Optional)Pipet 1ml of  the cultures into clean microcentrifuge tubes and  place the tubes on ice until  needed  for gel analysis or storage at  -20℃. These will serve as the non-induced control samples.     
6.   Add IPTG to a final concentration of 1 mM.  Optimal time for induction of the target protein may vary from 2-16 hours, depending on the protein.
7.   Incubate with shaking at 120 rpm at 37℃ for 2-4 hours. To determine the optimal time for induction of the target protein, it is recommended that a time course experiment be performed varying the induction from 2-16 hours.
8.   Place the culture on ice for 10 minutes. Harvest cells by centrifugation at 5,000 x g for 10
minutes at 4℃.
9.   Remove the supernatant and store the cell pellet at -20℃ (storage at lower temperatures is also acceptable). 

IPTG
Prepare a 1 M solution of IPTG (Isopropyl-β-D-thiogalactoside; Isopropyl-β-D-thiogalactopyranoside) bydissolving 2.38 g of IPTG in dd water and adjust the final volume to 10 ml. Filter sterilize before use.