The largest database of trusted experimental protocols

4 protocols using anti sumo1

1

Characterization of SUMO Pathway Proteins

Check if the same lab product or an alternative is used in the 5 most similar protocols
Primary rabbit antibodies included anti-actin (Sigma-Aldrich; A5060), anti-Daxx (Upstate; 07-471), anti-PIAS1 (LsBio; LS-B9173), anti-PIAS2 (LsBio; LS-C108717), anti-PIAS3 (LsBio; LS-C98795), anti-PIAS4 (LsBio; LS-C108719), anti-PML (Bethyl Laboratories; A301-167A), and anti-Sp100 (SpGH [37 (link)]) antibodies. Primary mouse antibodies included anti-ICP0 (11060 [38 (link)]), anti-ICP4 (58S [39 (link)]), anti-Daxx (AbD Serotec; MCA2143), anti-SUMO1 (Invitrogen; 33-2400), anti-SUMO2/3 (Abcam; ab81371), anti-UL42 (Z1F11 [40 (link)]), and anti-VP5 (DM165 [41 (link)]) antibodies. Primary sheep antibodies included anti-SUMO1 (Enzo Life Sciences; BML-PW0505) and anti-SUMO2/3 (Enzo Life Sciences; BML-PW0510) antibodies. Secondary antibodies included peroxidase-conjugated anti-mouse IgG (Sigma-Aldrich; A4416), DyLight 680- or DyLight 800-conjugated goat anti-rabbit or -mouse IgG (Thermo), and Alexa Fluor 488-, 555-, or 633-conjugated donkey anti-rabbit, -sheep, or -mouse IgG antibodies (Invitrogen).
+ Open protocol
+ Expand
2

Antibody Detection of Immunoprecipitated Receptor

Check if the same lab product or an alternative is used in the 5 most similar protocols
The primary antibody to detect immunoprecipitated receptor was: anti-MOR Ct aa 387–398 (GenScript Co.). Other primary antibodies used in this study were: anti-CaM (Millipore; #05-173), anti-GST (Cell Signaling; #2622), anti-HINT2 (Abnova; #H00084681-01), anti-RGSZ2(1 (link)) (Thermo Scientific; #PA1-25695), anti-RGSZ2(2 (link)) (aa 192-215; GenScript Co.) (14 (link)), anti-teneurin1 (Novus Biologicals; #NBP2-41315), anti-σ1R (Invitrogen; #42-3300), anti-SUMO1 (Enzo; #BML-PW9460), and anti-SUMO-2/3 (Enzo; #BML-PW9465). The anti-HINT1 antibody was raised in rabbits (Immunostep) against the peptide sequence GYRMVVNEGADGGG (93–106). All primary antibodies were detected by using the appropriate horseradish peroxidase-conjugated secondary antibodies.
+ Open protocol
+ Expand
3

Investigating HCMV UL44 Sumoylation

Check if the same lab product or an alternative is used in the 5 most similar protocols
HFF cells were infected with wild-type HCMV (UL44WT-Zeo) or HCMV containing UL44 K410A mutant (UL44-K410A-Zeo) at an MOI of 1. At 48 h post-transfection, total cell lysates were either directly analyzed by SDS-PAGE, or immunoprecipitated with anti-UL44 antibody which was covalently immobilized on Protein A/G beads by Pierce Crosslink Magnetic IP/Co-IP Kit (Thermo Fisher Scientific), then probed for UL44 or sumoylated proteins using anti-UL44 (Santa Cruz Biotechnology) or anti-SUMO1 (Enzo Life Science) antibodies, respectively.
+ Open protocol
+ Expand
4

Detecting Recombinant Protein Targets

Check if the same lab product or an alternative is used in the 5 most similar protocols
The primary antibodies to detect the recombinant proteins were anti-MOR Ct aa 387-398 (GenScript Co.), anti-Calmodulin (#05-173, Millipore,), anti-GST (#2622, Cell Signaling), anti-RGSZ2(1) (#PA1-25695, Thermo Scienti c), anti-RGSZ2(2) (aa 192-215; GenScript Co), anti-teneurin1 (#NBP2-41315, Novus Biologicals), anti-SUMO1 (#BML-PW9460, Enzo), anti-SUMO-2/3 (#BML-PW9465, Enzo). The anti-HINT1 antibody was raised in rabbits (Immunostep) against the peptide sequence GYRMVVNEGADGGG (93-106). All primary antibodies were detected using the appropriate horseradish peroxidase-conjugated secondary antibodies.
+ Open protocol
+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Sign up for free.
Registration takes 20 seconds.
Available from any computer
No download required

Sign up now

Revolutionizing how scientists
search and build protocols!