Over 2,000 TrueORF Clones are available for viral protein expressions
Over 2,000 TrueORF Clones are available for viral protein expressions
1. Quick thaw the cells in 37 C water bath and add to 10 ml of growth medium. Spin 5 min at 800 rpm to remove DMSO from freezing medium. DMSO is toxic to growing cells. Resuspend in 10 ml growth medium in 75 cm2 TC flask and place in 5% CO2/37 C incubator.
2. Plate approximately 5 x 105 cells into 60mm petri dishes. Wait until the cells reach 80% confluent.
3. Dilute 2-4 ug DNA of each construct to be transfected into 250 ul of OptiMEM or DMEM medium. Add 8 ul of Plus Reagent (Invitrogen # 11514-015) to the DNA/MEM mix. Let sit 15 min at room temperature.
4. Separately, mix 12 ul of Lipofectamine (Invitrogen # 18324-111) with 250 ul of OptiMEM or DMEM.
5. Mix DNA/MEM/Plus solution with Lipofectamine/MEM. Let sit 15 min at room temperature.
6. Remove growth medium from 60mm cell cultures. Rinse once with 2 ml OptiMEM or DMEM, replace with another 2 ml MEM to remove serum from the plate.
7. Add preincubated DNA/Plus/Lipofectamine/MEM solution to the cells. Mix gently.
8. Grow cells 3 hr – overnight. Add 2.5 ml N2a medium and continue culture.
If developing stable transfectants, add G418 (Gibco/Life Tech # 1181-031) to the growth medium to select for positive cells. Use at 400-800 ug/ml for selection of clones, and 200-400 ug/ml for maintenance.
9. 48 hours post transfection, harvest the cells for the future assay.
DMEM, high glucose, w/L-gluatmine Gibco # 11965-092 250ml
Fetal bovine serum, qualified Gibco # 26140-079 50ml
OptiMEM 1 medium Gibco # 31985-070 250ml
Penicillin-Streptomycin Gibco # 15140-122 5ml
Filter to 0.2 um. Stable for several months at 4 C.
1. Solutions and reagents
1.2. Ethanol, anhydrous denatured, histological grade (100%, 95%, 70%, 50%)
1.3. Washing buffer/TBST: 1X TBS/0.1% Tween-20, pH to 7.6.
1.4. Distilled water (dH 2O)
1.5. Antigen Retrieval Solution: 0.01M Sodium Citrate Buffer, pH 6.0
To prepare Antigen Retrieval stock solutions:
- 10X Stock: Dissolve 29.4 g sodium citrate trisodium salt dihydrate (C 6H 5Na 3O 7 2H 2O)
in 1 liter of dH2O. Add 5mL Tween-20.
- 1X Working Solution: Mix 200mL 10X stock with 1800mL dH2O; pH to 6.0
1.6. 3% Hydrogen Peroxide
1.7. Blocking Buffer: 10% serum in PBS (serum origin depends on the host of the secondary antibody)
1.8. Primary Antibody Diluent: 5% serum in PBS (serum origin depends on the host of the secondary antibody)
1.10. Permanent Mounting Medium
2. IHC Protocol
2.1.1. Heat slides in an oven at 65 °C for 1 hour.
2.1.2. De-paraffinize/hydrate using the following series of washes: two Xylene washes (3 min each), followed by two 100% ethanol rinses (3 min each), followed by 95% ethanol, 70% ethanol, 50% ethanol, 30% ethanol, followed by TBST wash for 3 min on a shaker.
2.2. Antigen Retrieval
This is recommended Heat Induced Epitope Retrieval (HIER) using Decloaking Chamber/Pressure Cooker. Hot water bath or Microwave with temperature sensor can be also used (protocol would vary depending on the method used).
2.2.1. Add 500 ml of dH 2O to Decloaker/Pressure Cooker.
2.2.2. Immerse slides into staining dish containing Antigen Retrieval Solution. Place staining dish into decloaking chamber.
2.2.3. Program to run for 30 seconds at 125° C, followed by 10 seconds at 90° C.
2.2.4. Let it cool down to room temperature (10 – 20 minutes).
2.2.5. Removes slides and rinse in TBST.
2.2.6. Proceed to Staining step.
2.3.1. Wash slides with TBST for 3 min on a shaker.
2.3.2. Inactivate endogenous peroxidase by covering tissue with 3% hydrogen peroxide for 5 min.
2.3.3. Wash slides three times with TBST (3 min each on a shaker).
2.3.4. Block slides with the blocking solution for 1 hour.
2.3.5. Dilute primary antibody in primary antibody diluent per recommendation on data sheet.
2.3.6. Apply primary antibody to each section and incubate overnight in the humidified
chamber (4 °C).
2.3.7. Wash slides three times with TBST (3 min each on a shaker).
2.3.8. Apply to each section secondary HRP-conjugated anti-rabbit antibody diluted in the blocking solution per manufacturer’s recommendation; incubate for 30 min at room temperature.
2.3.9. Wash slides three times with TBST (5 min each on a shaker).
2.3.10. Add freshly prepared DAB substrate to the sections and incubate until stain develops (generally 1 min).
2.3.11. Rinse sections with water.
2.3.12. Counterstain with Hematoxylin (generally 10 seconds).
2.3.13. Rinse sections with water.
2.3.14. Dehydrate samples using two washes with 100% Ethanol (3 min each), followed by two rinses with Xylene (3 min each).
2.3.15. Mount coverslips on slides using permanent mounting medium
OriGene now offers the service to generate Mass Spectrometry (MS) standards for 6,000 human proteins. Produced in human HEK293T cells and labeled with [U- 13C6, 15N4]-L-Arginine and [U- 13C6, 15N2]-L-Lysine, the full length proteins with appropriate post-translational modifications are the best identification and quantification standards.
Supriority of OriGene’s MS standards:
1. Do a kill-curve to find out the lowest dose to kill your cells (4-7 days for puromycin). You can do that any time. You just need to know what concentration to use to select for your stable transfected clones.
Split your cells at 1:10 the day before the selection. Change the medium with different concentration of puromycine every 2 to 3 days. The normal conc. used for Puromycin is from 0.1 ug/ml to 10 ug/ml. So you can pick up a series of conc. within this range. For example, you can use 6 well plates, with each well containing a different conc. of puromycin (0, 0.1, 0.5, 1, 2, 10). You can pick more point if you want, so that you can get more accurate data. Check your cells every day, after 1 week, find the lowest dose that kill all your cells (100%). That’s the concentration you want to use for selection.
2. Perform a transfection with the plasmid containing Puro resistant gene. Twenty-four hrs post-transfection, passage the cells at 1:10 into fresh growth medium containing puromycin at the concentration you found from step 1. A mock transfection should be performed in parallel as a control. Grow and passage the cells as necessary (usually 2-3 days), maintaining selection pressure by keeping puromycin in the growth medium. After 1-2 weeks, a large number of the cells will be killed; the cells that remain growing in the selective medium have retained the expression plasmid, which stably integrates into the genome of the targeted cells. Monitor the mock control to ensure the cells are dying, no cells attached at the bottom.
3. If you pool all the colonies, that is your stable pool. If you isolate individual colony, that is your individual clones. For isolation of individual colony, there are several commercial tools to do that. You can also keep on diluting your stable transfected cells to the point that you can assume every well only get one colony. Continue growing these cells in selection medium for 1-2 additional passages. At this time, each well contains a clonal population of stably transfected cells, which can be maintained in normal growth medium without the selection pressure of puromycin (although you may wish to grow the cells under “light pressure”, lower concentration of puromycin). These populations can be used for experiments or stored under liquid nitrogen in growth medium with 10% DMSO and 20% FBS for future use.