THY1 Knockout Cell Line (LLC) Company | THY1 KO Cell Line LLC Price - EDITGENE

Enzymes

  Cas12

  Cas13

  Cas9
RNA

  gRNA

  crRNA

  IND gRNA

  GMP gRNA
CRISPR Gene Editing Kit

  CRISPR Knockout Kit

  Transfection Kit

  Lentiviral Packaging Kit

  CRISPR Point Mutation Kit

  piggyBac Transposon Kit
Whole-Category Cell Line

  KO Cell Line

  Point Mutation Cell Line

  Overexpression Cell Line

  Cas9 Expressing Cell Line

  GFP Cell Line

  Luciferase Cell Line

  Wild Type Cell Line

  Others
CRISPR Library

  Plasmid Libraries

●  CRISPR KO ●  CRISPRa ●  CRISPRi

  Library virus

●  CRISPR KO ●  CRISPRa ●  CRISPRi
Plasmid

  KO Plasmid

  PE Plasmid

  OE Plasmid

  Other Plasmids
CRISPR Detection

  crRNA

  Isothermal DNA Kit

  Isothermal RNA Kit

  Test Strips

  Probes

THY1 knockout cell line (LLC)

立即询价

货号:

EDJ-KQ52

基因名称:

THY1

基因ID:

7070

规格:

1×10⁶cells

细胞形态:

semi-adherent semi-suspension

产品介绍

THY1 Knockout Cell Line (LLC) is an exclusive upgraded CRISPR/Cas9 system-mediated gene knockout cell, with the advantages of Optimized Strategy Design, Efficient Cell Transfection, High-Performotion Cas9 Protein and Hassle-Free Cell Selection.

产品属性

Cat.No.	EDJ-KQ52
Product Name	THY1 Knockout Cell Line (LLC)
Gene	THY1
Gene Id	7070
Morphology	semi-adherent semi-suspension
Passage Ratio	1/4-1/3,2 days
Complete Culture Medium	DMEM + 10% FBS
Freezing Medium	95% Complete culture medium + 5% DMSO

Cell recovery

Note: After receiving the cells, please store in liquid nitrogen. Take it out 10 minutes before recovering cells and place it at -80 ℃ to allow the liquid nitrogen in the tube to evaporate
1. Preheat the water bath and complete culture medium at 37 ℃;
2. Add 6mL of complete culture medium to a 15mL centrifuge tube;
3. Gently swirl the cryopreservation tube in a 37 ℃ water bath until a small piece of ice remains in the cryopreservation tube, please thaw it within 1 minute, and the cap should not touch water;
4. In the ultra clean bench, before opening the cap, wipe the outside of the cryopreservation tube with 75% alcohol;
5. Transfer all the liquid with a pipette to a centrifuge tube of preheated complete culture medium;
6. Rinse the cryopreservation tube with 1mL of complete culture medium to collect residual cells;
7. Centrifuge the cell suspension at 1100 rpm for 4 minutes (centrifugation speed and time depend on cell type);
8. After centrifugation, check if the supernatant is clear and if there is cell pellet at the bottom; inside the hood, carefully pour out the supernatant, add 1mL of complete culture medium, gently resuspend the cell pellet;
9. Evenly seed cells into a T25 flask or culture container with an equivalent bottom area. Add a sufficient amount of complete culture medium, and the total amount of culture medium in a T25 flask shall not be less than 6mL (the actual size of the flask depends on the number of cells frozen in the cryopreservation tube);
10. Gently mix the cells well and place them in a 37 ℃, 5% CO2, saturated humidity incubator (the culture environment depends on cell type and culture medium);
11. Observe the cell status on next day:
(1) If the adherent cells adhere well, change fresh complete culture medium; If the cells are observed to be in a round and bright shape but not adhering to the plate, continue cultivation for 24 hours. Afterwards, based on the growth status of the cells, replace the complete culture medium every 2-3 days, observe the cells, and passage cells when confluence rate >80%. If the cell growth is slow or the confluence rate is low, the frequency of medium change can be reduced;
(2) When recovering suspension cells, place them in a relatively small container and use a culture medium containing 20% serum for recovery. If the suspended cells are in good condition, change fresh complete culture medium; If the cell status is poor and appears grayscale, it can be further cultured for 72 hours. Change fresh medium if observe live cells. If no significant changes are observed, please contact us for after-sales service in a timely manner.

Passage method

1. View cultures using an inverted phase contrast microscope to assess the degree of confluency and confirm the absence of bacterial and fungal contaminants. Give the flask a gentle knock first, this may dislodge the cells from the flask and remove the need for a trypsinisation step loss of some cells due to associated washes;
2. Decant medium containing non-adherent cells into a sterile centrifuge tube and retain;
3. Wash any remaining attached cells with PBS without Ca2+/Mg2+ using 1-2ml for each 25cm2 of surface area. Retain the washings;
4. Pipette trypsin/EDTA onto the washed cell monolayer using 1ml per 25cm2 of surface area. Rotate flask to cover the monolayer with trypsin. Decant the excess trypsin;
5. Return flask to incubator and leave for 2-10 minutes;
6. Examine the cells using an inverted microscope to ensure that all the cells are detached and floating. The side of the flasks may be gently tapped to release any remaining attached cells;
7. Transfer the cells into the centrifuge tube containing the retained spent medium and cells;
8. Centrifuge the entire cell suspension at 150 x g for 5 minutes;
9. Remove the supernatant and re-suspend the cell pellet in a small volume (10-20ml) of fresh culture medium. Count the cells;
10. Pipette the required number of cells into a new labelled flask and dilute to the required volume using fresh medium;
11. Repeat this process every 2-3 days as necessary.