BD, 610028, BD Transduction Laboratories™ Purified Mouse Anti-Phospholipase Cγ1

Reactivity: Human (QC Testing), Mouse, Rat, Dog, Chicken (Tested in Development)
Isotype: Mouse IgG1
Immunogen: Cow PLCγ1 N-terminal region Peptide
Application: Western blot (Routinely Tested), Bioimaging, Immunohistochemistry, Immunoprecipitation (Tested During Development)
Target Molecular Weight: 148 kDa
Concentration: 250 µg/ml
RRID: AB_397446
Storage Buffer: Aqueous buffered solution containing BSA, glycerol, and ≤0.09% sodium azide.
Regulatory Status: RUO
Preparation And Storage: Preparation And Storage Store undiluted at -20°C. The monoclonal antibody was purified from tissue culture supernatant or ascites by affinity chromatography.
Recommended Assay Procedures: Recommended Assay Procedures Western blot: Please refer to http://www.bdbiosciences.com/pharmingen/protocols/Western_Blotting.shtml Recommended Protocol for Bioimaging: 1. Seed the cells in appropriate culture medium at an appropriate cell density in a BD Falcon™ 96-well Imaging Plate (Cat. No. 353219), and culture overnight to 48 hours. 2. Remove the culture medium from the wells, and wash (one to two times) with 100 µl of 1× PBS. 3. Fix the cells by adding 100 µl of fresh 3.7% Formaldehyde in PBS or BD Cytofix™ fixation buffer (Cat. No. 554655) to each well and incubating for 10 minutes at room temperature (RT). 4. Remove the fixative from the wells, and wash the wells (one to two times) with 100 µl of 1× PBS. 5. Permeabilize the cells using either cold methanol (a), Triton™ X-100 (b), or Saponin (c): a. Add 100 µl of -20°C 90% methanol or -20°C BD™ Phosflow Perm Buffer III (Cat. No. 558050) to each well and incubate for 5 minutes at RT. b. Add 100 µl of 0.1% Triton™ X-100 to each well and incubate for 5 minutes at RT. c. Add 100 µl of 1× Perm/Wash buffer (Cat. No. 554723) to each well and incubate for 15 to 30 minutes at RT.  Continue to use 1× Perm/Wash buffer for all subsequent wash and dilutions steps. 6. Remove the permeabilization buffer from the wells, and wash one to two times with 100 µl of appropriate buffer (either 1× PBS or 1× Perm/Wash buffer, see step 5.c.). 7. Optional blocking step:  Remove the wash buffers, and block the cells by adding 100 µl of blocking buffer BD Pharmingen™ Stain Buffer (FBS) (Cat. No. 554656) or 3% FBS in appropriate dilution buffer to each well and incubating for 15 to 30 minutes at RT. 8. Dilute the antibody to its optimal working concentration in appropriate dilution buffer.  Titrate purified (unconjugated) antibodies and second-step reagents to determine the optimal concentration.  If using a Bioimaging Certified antibody conjugate, dilute it 1:10. 9. Add 50 µl of diluted antibody per well and incubate for 120 minutes at RT.  Incubate in the dark if using fluorescently labeled antibodies. 10. Remove the antibody, and wash the wells three times with 100 µl of wash buffer.  An optional detergent wash (100 µl of 0.05% Tween in 1× PBS) can be included prior to the regular wash steps. 11.   If the antibody being used is fluorescently labeled, then move to step 12.  Otherwise, if using a purified unlabeled antibody, repeat steps 8 to 10 with a fluorescently labeled second-step reagent to detect the purified antibody. 12. After the final wash, counter-stain the nuclei by adding 100 µl of a 2 µg/ml solution of Hoechst 33342 (eg, Sigma-Aldrich Cat. No. B2261) in 1× PBS to each well at least 15 minutes before imaging. 13. View and analyze the cells on an appropriate imaging instrument. Recommended filters for the BD Pathway™ instruments are: Instrument Excitation Emission Dichroic BD Pathway 855 488/10 515 LP Fura/FITC BD Pathway 435 482/35 536/40 FF506