Jul 14, 2023
Nuclei Isolation for 10X Multiome Sequencing
- 1Princeton Neuroscience Institute
Protocol Citation: Lakme Caceres 2023. Nuclei Isolation for 10X Multiome Sequencing. protocols.io https://dx.doi.org/10.17504/protocols.io.kxygx3pqkg8j/v1
License: This is an open access protocol distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited
Protocol status: Working
We use this protocol and it's working
Created: July 14, 2023
Last Modified: July 14, 2023
Protocol Integer ID: 85032
Abstract
This protocol is for isolating nuclei for 10X multiome sequencing.
Guidelines
Keep tissue/nuclei on ice as much as possible.
Prepare Stock Solutions
Prepare Stock Solutions
Make 20 mL 10% BSA by combining 2 mL of BSA with 18 mL of MilliQ water in a 50 mL falcon tube. (4°C - 2 weeks)
Make 20 mL 10% Triton X-100 by combining 18 mL MilliQ water with 2 mL Triton X-100 in a 50 mL tube. Vortex and then incubate at room temperature for 20 minutes. Filter it through a 0.22 μm filter with a syringe into a clean 50 mL tube. (4°C - 1 month)
Make 250 mL Nuclear Isolation Media by filling a 250 mL bottle with 200 mL of MilliQ water and then adding 2.5 mL 1M Tris, 6.26 mL 1M KCl, 1.25 mL 1M MgCl2, and 21.45 g Sucrose. Shake until sucrose is dissolved then fill to 250 mL with MilliQ water. (4°C - 2 weeks)
Prepare Fresh Solutions
Prepare Fresh Solutions
Make 3 mL Homogenization Buffer per sample by adding 2.895 mL Nuclear Isolation Media (filtered via syringe) to a 5 mL eppendorf. Then add 3 μL 100 mM DTT and 30 μL 10% Triton X-100. Add 15 uL RNAsin and invert to mix. Store on ice.
Make 200 uL Blocking Buffer per sample by dividing your total desired volume of blocking buffer by 10 to get the amount of 10% BSA in uL. Add this amount to a tube and then fill the remainder with 1X PBS.
Homogenization
Homogenization
Clean dounce, scalpel, and forceps using MilliQ water, ethanol, RNase Zap, then MilliQ again. The red-tape forceps are for unfixed tissue.
Get tissue sample from -80°C freezer and place on dry ice. Weigh it on a sterile, tared weigh boat.
Add tissue to dounce and push it to the bottom using 1 mL of Homegenization Buffer and the pestle. Homogenize the tissue without creating bubbles. Then add the remaining 2 mL of the Homogenization Buffer and continue to dounce until homogenized.
Pass all of the nuclei suspension through three FlowMi filters, 1000 μL at a time into a new 5 mL eppendorf.
Centrifuge at 900 g/rcf for 10 minutes at 4°C.
Discard the supernatant and resuspend the pellet in 200 μL Blocking Buffer. Incubate for 10 minutes on ice.
Cell Count
Cell Count
Add 9 uL of sample to a PCR tube and then add 1 uL of acridine orange.
If sample is very concentrated, instead add 2 uL sample to 2 uL of acridine orange and 16 uL 1X PBS.
Pipette mix and then add 10 uL to a three-chamber cell counting chip and make note of the channels used (A, B, and/or C).
On the cell counter, select Fluorescence Cell Counting -> Cell Lines & Primary Cells, Advanced-> Protocol -> and then choose "NUCLEI" from the list of protocols. Load the protocol.
If the sample is very concentrated and you are adding 2 uL, select Fluorescence Cell Counting -> Cell Lines & Primary Cells-> Protocol -> and then choose "NUCLEI" from the protocol list. Load the protocol.
Then go to Settings and choose the appropriate number of channels.
Then hit "Count" and then "Start Count."
When the cell count is complete, you will get a reading in cells/mL. Convert this to cells/uL by dividing this number by 1,000.
Dilute this nuclei stock to a concentration of 7,000 nuclei/uL.
Example:
(2,000 n/uL)(500 uL) = (7,000 n/uL)(x uL)
x = 2,286 uL
2,286 uL - 498 uL remaining after cell count = 1,788 uL blocking buffer needed to add to sample
If there are channels left on the cell counter chip, mark the used channels on the back and place it back in the drawer for future use.
Proceed with step 1 of the 10X Multiome protocol.