Human ANP32B Knockdown Cell Line (Wb-Validated) #C61425

ANP32B; Acidic Nuclear Phosphoprotein 32 Family Member B; PHAPI2; APRIL; Acidic Protein Rich In Leucines; SSP29; Acidic (Leucine-Rich) Nuclear Phosphoprotein 32 Family, Member B; Acidic Leucine-Rich Nuclear Phosphoprotein 32 Family Member B; Putative HLA-DR-Associated Protein I-2; Silver-Stainable Protein SSP29

NCBI Gene Entry: 10541

1. Human ANP32B Knockdown Cell Line (Wb-Validated)

2 . Wild-type cell line

Human cell line supplied by the client

RT-qPCR

Western Blotting (WB)

Shipped on Dry Ice.

Store at liquid nitrogen for 1 year.

This knockdown cell line should be paired with wild-type cell line for use.

The following protocol was used to generate mRNA knockdown cells:

1.Release 0.5 million 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 cells as a negative control.

11.Allow puromycin selection for 48 h. Almost all wild-type 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.

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.