hnRNP M1-M4 Antibody (1D8) - BSA Free

hnRNP M1-M4 Antibody (1D8):
Day 1 Cell Growth

1. Grow cells directly on a 10-well microscope slide (Cel-Line Associates, 10-well, 7MM, HTC autoclavable slides, Catalog# 10-7) in 15 cm cell culture plates, overnight.
- The flatter the cells, the better the IF.
- HeLa JW36 cells are a better positive control than HeLa S3 cells.

Day 2 Fixation

2. Rinse slides 3x with PBS (swirl ~200 ml into a 250 ml beaker).
3. Fix slide in Coplin jar for 30 minutes at RT, in 2% formaldehyde (MeOH-free, 10% ultrapure, EM grade).
- Formaldehyde is diluted in PBS.
4. Rinse slides 3x with PBS (swirl 200 ml into a 250 ml beaker).
5. Incubate for 3 minutes in acetone at 20C (acetone stock should be kept at 20 degrees C).
6. Rinse slides 3x with PBS (swirl 200 ml into a 250 ml beaker).
7. Store fixed slides up to 1 week in PBS + 0.2% azide, in Coplin jar.

Same Day Immunofluorescence

8. Rinse slide 1x in PBS.
9. Dry with Kimwipe (or equivalent) and wipe around well with a cotton-tipped applicator.

**This drying procedure is repeated at each subsequent step, but be careful not to dry out the well

10. Add 10 ul of 3% BSA in PBS, per well, and pre-incubate for 15 minutes at RT in a humidifier chamber.
11. Wash slide 1x in PBS, add 10 ul of anti-RNP M1-M4 and incubate 60 minutes in chamber at RT.
12. Rinse slides 3x with PBS.
13. Add 10 ul of appropriate secondary antibody and incubate for 30 minutes at RT.
14. Rinse slides 3x in PBS.
15. Mount slides with IF mounting media and seal with clear nail polish.
16. Slides can be stored up to 1 week at 20C, in Revco box.

hnRNP M1-M4 Antibody (1D8):
Western Blot Procedure Guide for NB 200-314 Monoclonal Anti-RNP M1-M4

1) Wet Nitrocellulose membrane with PBS + NP40 [PN].
2) Pour off PN.
3) Dilute anti-RNP M1-M4 (catalog# NB 200-314) in 5%NFDM + NP40.
4) Incubate the primary antibody with the membrane for 1 hour, at room temperature (RT), gently rocking.
5) Wash 1x with PN for 10 minutes. Wash 2x with PN for 5 minutes, each.
6) Dilute anti-mouse-HRP (Amersham) in 5%NFDM + NP40 at 1:5,000.
7) Incubate the secondary antibody with the membrane for 45 minutes, at RT, gently rocking.
8) Wash 1x with PN for 10 minutes. Wash 2x with PN for 5 minutes, each.
9) Wash 1x with PBS for 5 minutes.
10) Develop using Amersham ECL components.

**NOTE: HeLa nuclear cell extracts can be used as a positive control for this antibody.