Product Type: | Rabbit polyclonal IgG, primary antibodies |
---|---|
Species reactivity: | Species independent |
Applications: | WB, ELISA, IF-Cell |
Clonality: | Polyclonal |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | 1*TBS (pH7.4), 0.2% BSA, 50% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Immunogen affinity purified. |
Isotype: | IgG |
Immunogen: | Recombinant protein within mCherry 1-236aa. |
Positive control: | Recombinant mCherry protein lysates. |
Recommended Dilutions:
WB ELISA IF-Cell |
1:5,000 1:1,000-1:5,000 1:10,000 |
Uniprot #: | SwissProt: X5DSL3 AnaplasmaMarginale |
Fig1:
Western blot analysis of mCherry on different lysates with Rabbit anti-mCherry antibody (HA500049) at 1/5,000 dilution. Lane 1: 293T transfected with empty control cell lysate Lane 2: 293T transfected with mCherry cell lysate Lysates/proteins at 5 µg/Lane. Exposure time: 4 seconds; ECL: K1801; 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 (HA500049) 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. |
|
Fig2: ELISA analysis of with anti-mCherry antibody. Antigen (1 μg/mL). The antigen was used as the coating antigen, and the anti-mCherry antibody was used as the capture antigen for ELISA. | |
Fig3:
Immunocytochemistry analysis of HeLa cells transfected with or without mCherry labeling mCherry with Rabbit anti-mCherry antibody (HA500049) at 1/10,000 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 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-mCherry antibody (HA500049) at 1/10,000 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. |