GALC Recombinant Rabbit Monoclonal Antibody [PSH03-45] - BSA and Azide free

This data was developed using HA722004, the same antibody clone in a different buffer formulation.
Western blot analysis of GALC on different lysates with Rabbit anti-GALC antibody (HA722004) at 1/5,000 dilution.

Lane 1: 293T cell lysate
Lane 2: A375 cell lysate
Lane 3: A549 cell lysate
Lane 4: HepG2 cell lysate
Lane 5: NIH/3T3 cell lysate
Lane 6: PC-12 cell lysate
Lane 7: Mouse brain tissue lysate
Lane 8: Mouse testis tissue lysate
Lane 9: Rat brain tissue lysate
Lane 10: Rat testis tissue lysate

Lysates/proteins at 20 µg/Lane.

Predicted band size: 77 kDa
Observed band size: 60 kDa

Exposure time: 43 seconds;

4-20% SDS-PAGE gel.

Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA722004) at 1/5,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.

This data was developed using HA722004, the same antibody clone in a different buffer formulation.
Immunocytochemistry analysis of A549 cells labeling GALC with Rabbit anti-GALC antibody (HA722004) at 1/100 dilution.

Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-GALC antibody (HA722004) at 1/100 dilution in 1% BSA in PBST overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.

Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.