| Product Name |
WB-Validated RACK1 Lentiviral shRNA Knockdown Kit |
| Aliases |
RACK1; Receptor For Activated C Kinase 1; GNB2L1; H12.3; Guanine Nucleotide Binding Protein (G Protein), Beta Polypeptide 2-Like 1; Guanine Nucleotide-Binding Protein Subunit Beta-Like Protein 12.3; Guanine Nucleotide-Binding Protein Subunit Beta-2-Like 1; Cell ProlifeRation-Inducing Gene 21 Protein ; Receptor Of Activated Protein C Kinase 1; Small Ribosomal Subunit Protein RACK1; Human Lung Cancer Oncogene 7 Protein ; Gnb2-Rs1; HLC-7; Protein Homologous To Chicken B Complex Protein, Guanine Nucleotide Binding; Guanine Nucleotide Binding Protein Beta Polypeptide 2-Like 1; Receptor Of Activated Protein Kinase C 1; Receptor For Activated C Kinase; ProlifeRation-Inducing Gene 21; Lung Cancer Oncogene 7; PIG21(多GNB2-RS1) |
| Background |
Gene Name: RACK1
NCBI Gene Entry: 10399
|
| Storage |
Store at -80 °C for one year. |
| Kit Components |
1. WB-Validated RACK1 shRNA lentiviral particles (4 mL)
2. Non-Target shRNA lentiviral particles (4 mL)
3. Verification Tool: KD-Validated Anti-RACK1 Rabbit mAb #61248 (5 μL) |
| Tested Cell Line |
HeLa |
| Validation Methods |
RT-qPCR; Western Blotting (WB) |
| Shipping |
Shipped with dry ice. Immediately store the product in a standard freezer at -80°C upon receipt. |
| Instructions For Use |
The following protocol uses HeLa cell as an example assuming your cell culture medium is DMEM-based.
1.Release 0.5 million HeLa cells into a 35 mm tissue culture dish in 2 mL of the growth medium (DMEM containing 10% FBS and 1% pen/strep). Cell density should reach 50-60% confluence the following day.
2.24 h after cell release, pre-warm the shRNA lentiviral medium to 37°C.
3.Discard 1 mL of the original growth medium of the 35 mm dish.
4.Using a serological pipette, gently mix the lentiviral solution 3 times.
5.Carefully add 1 mL of the lentiviral solution to the well. Tip: To prevent splashing, add the solution to the dish along the wall.
6.Add a polybrene stock solution to the culture medium at a final concentration of 5 μg/mL. Gently swirl the dish to mix.
7.48 h after cell release, without discarding the original medium, add another 1 mL of lentiviral medium directly into the dish.
8.Add an additional polybrene stock solution into the dish to obtain a final concentration of 5 μg/mL. Tip: Now, the medium in the dish should be a total of 3 mL.
9.72 h after cell release, cells may reach confluence. Trypsinize the cells off the 35 mm dish and culture those cells in a 60 mm dish.
10.Add puromycin to the dish at a final concentration of 4 μg/mL. Tip: To assess the efficacy of puromycin selection, culture a dish of wild-type HeLa cells as a negative control.
11.Allow puromycin selection for 48 h. Almost all wild-type HeLa cells should die, while the dish infected with lentiviruses should have some remaining cells.
12.Replace the medium with regular growth medium without puromycin and allow the cells to grow to confluence before harvesting or staining. |
| Note |
1. This product is for research use only.
2. This product is only supplied to end users.
3. Do not use this product for commercial. |
