Product Type: | Rabbit polyclonal IgG, primary antibodies |
---|---|
Species reactivity: | Human, Rat |
Applications: | WB, IF-Cell |
Clonality: | Polyclonal |
Form: | Liquid |
Storage condition: | Store at +4℃ after thawing. Aliquot store at -20℃. Avoid repeated freeze / thaw cycles. |
Storage buffer: | PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide. |
Concentration: | 1ug/ul |
Purification: | Immunogen affinity purified. |
Molecular weight: | Predicted band size: 49 kDa |
Isotype: | IgG |
Immunogen: | Recombinant protein within Human Urokinase 10- 200 aa |
Positive control: | PC-3M cell lysate, MCF-7 cell lysate, LANCAP cell lysate, rat kidney tissue lysate, rat stomach tissue lysate, PC-3M. |
Subcellular location: | Secreted. |
Recommended Dilutions:
WB IF-Cell |
1,000-2,000 1:200 |
Uniprot #: | SwissProt: P00749 Human | P29598 Rat |
Alternative names: | ATF ATF uPA BDPLT5 Plasminogen activator Plasminogen activator urinary Plasminogen activator urokinase PLAU QPD u PA U plasminogen activator u-PA U-plasminogen activator uPA URK UROK_HUMAN Urokinase plasminogen activator Urokinase type plasminogen activator Urokinase type plasminogen activator precursor Urokinase-type plasminogen activator chain B hide |
Fig1:
Western blot analysis of Urokinase on different lysates with Rabbit anti-Urokinase antibody (HA500429) at 1/2,000 dilution. Lane 1: PC-3M cell lysate (10 µg/Lane) Lane 2: MCF-7 cell lysate (10 µg/Lane) Lane 3: LANCAP cell lysate (10 µg/Lane) Lane 4: Rat kidney tissue lysate (20 µg/Lane) Lane 5: Rat stomach tissue lysate (20 µg/Lane) Predicted band size: 49 kDa Observed band size: 56 kDa Exposure time: 2 minutes; 10% 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 (HA500429) at 1/2,000 dilution was used in 5% NFDM/TBST at room temperature for 2 hours. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1:300,000 dilution was used for 1 hour at room temperature. |
|
Fig2:
Immunocytochemistry analysis of PC-3M cells labeling Urokinase with Rabbit anti-Urokinase antibody (HA500429) at 1/200 dilution. Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at 37℃. Cells were then incubated with Rabbit anti-Urokinase antibody (HA500429) at 1/200 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. 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™ 647, HA1127) was used as the secondary antibody at 1/1,000 dilution. |