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This protein carries a polyhistidine tag at the C-terminus.
The active form of Human PLAU is a disulfide-linked heterodimer composed of long chain A (Ser 21 - Phe 177) and chain B (Ile 179 - Leu 431) with calculated MW of 17.8 kDa and 29.2 kDa. The long chain A is further cleaved to yield a short chain A (Lys 156 - Phe 177) and N-terminal fragment (Ser 21 - Lys 155) with calculated MW of 15.3 kDa. The protein migrates as 17 kDa (N-terminal fragment), 32-35 kDa (chain B) and 45-50 kDa (long chain A & chain B) under non-reducing (NR) condition (SDS-PAGE) due to glycosylation.
>90% as determined by SDS-PAGE.
Lyophilized from 0.22 μm filtered solution in 25 mM HEPES, 150 mM NaCl, pH7.5 with trehalose as protectant.
Contact us for customized product form or formulation.
Please see Certificate of Analysis for specific instructions.
For best performance, we strongly recommend you to follow the reconstitution protocol provided in the CoA.
For long term storage, the product should be stored at lyophilized state at -20°C or lower.
Please avoid repeated freeze-thaw cycles.
This product is stable after storage at:
Human PLAU, His Tag (activated by trypsin) on SDS-PAGE under non-reducing (NR) condition. The gel was stained with Coomassie Blue. The purity of the protein is greater than 90%.
Measured by it's ability to cleave a peptide substrate, N-carbobenzyloxy-Gly-Gly-Arg-7-amido-4-methylcoumarin (Z-GGR-AMC). The specific activity is >2,000 pmol/min/µg, as measured under the described conditions (QC tested).
Emerging VoCs, Omicron, Delta, Beta, Alpha mutants and so on, including RBD, S trimer, S1, NTD, NP, etc. These mutants are of high purity and bioactivity and can be used to evaluate the efficacy of the antibodies and vaccination.
ACROBiosystems developed a series of GMP grade cytokines under the GMP grade quality management system. Those products are all suitable for T/NK cell generation, activation, and proliferation in cell therapy research.
50+ targets designed for CAR detection, including PE/FITC/biotin labeled proteins. The key reagents for CD19 and BCMA were FDA DMF filed which can support your IND, NDA and BLA process.
GMP grade cytokines, reagents for cell activation, gene edition, DNA/RNA removal, etc. Particularly focus on product design, quality control and solution-based support to link each phase of your cell and gene therapy journey.
Full length multi-pass TPs with stabilized structure and high bioactivity for immunization, antibody screening, cell based assay and CAR detection, including hot CD20, Claudin 18.2, CD133, GPRC5D,CCR8, CCR5, etc.
CD3 proteins and a collection of for bispecific antibody development which are of high specificity and bioactivities and suitable for immunization, antibody screening.
A series of immune checkpoints including classic co-inhibitory and co-stimulatory receptors. The comprehensive catalog contains 100+ targets with various species and tags, and the high-quality proteins are in good batch-to-batch consistency.
To meet the needs of ADCs development, ACROBiosystems can provide: A variety of high-quality target proteins; MMPs/Cathepsin/uPA for cleavable linker; Anti-payload antibodies & anti-idiotypic antibodies for immunogenicity and PK analysis; SPR/BLI analytical and ADA development service.
Comprehensive collection of Fc receptor proteins, including their common variants, which can help expedite your antibody development.
The MABSOL biotinylated protein collection includes more than a hundred commonly studied drug targets and biomarker proteins.
Comprehensive cytokines including IL families, growth factors, chemokines, TNFs, etc. These products are HEK293 expressed and nearly in authentic structure, high purity and bioactivity, cell based assay/SPR/BLI verified.
To support preclinical/clinical immunogenicity and PK analysis, ACROBiosystems has developed a series of high-affinity anti-idiotypic antibodies. Our pipeline covers five hot targets including adalimum*b, rituxim*b, cetuxim*b, trastuzum*b, and bevacizum*b.
English Name | Research Code | Research Phase | Company | First Brand Name | First Approved Country | First Indication | First Approved Company | First Approved Date | Indications | Clinical Trials |
---|---|---|---|---|---|---|---|---|---|---|
Urokinase biosimilar (Sedico) | Approved | Sedico | Angikinase | Egypt | Pulmonary Embolism; Myocardial Infarction; Thromboembolism | Sedico | 2014-01-01 | Pulmonary Embolism; Myocardial Infarction; Thromboembolism | Details | |
Nasaruplase | GE-0943 | Approved | Mitsubishi Pharma Corp | Tomieze, Thrombolyse | Japan | Myocardial Infarction; Venous Thrombosis | Mitsubishi Pharma Corp | 1992-01-01 | Myocardial Infarction; Venous Thrombosis | Details |
Tisokinase | AK-124 | Approved | Kowa Co Ltd, Asahi Kasei Corp | Plasvata, Hapase | Japan | Myocardial Infarction; Thrombosis | null | 1991-01-01 | Myocardial Infarction; Thrombosis | Details |
Urokinase biosimilar (Bharat Serums & Vaccines) | U-FRAG | Approved | Bharat Serums And Vaccines Ltd | Pulmonary Embolism | Details |
English Name | Research Code | Research Phase | Company | Indications | Clinical Trials |
---|---|---|---|---|---|
Urokinase biosimilar (Suzhou Landing Biological Pharmaceutical) | Phase 3 Clinical | Suzhou RxD Biopharmaceutical Co Ltd | ST Elevation Myocardial Infarction | Details | |
WX-UK1 | WX-UK1 | Wilex | Details | ||
Gallium-68 NOTA AE105 (Curasight) | CS-001; 68Ga-NOTA-AE105 | Phase 2 Clinical | Curasight Aps | Head and Neck Neoplasms; Glioblastoma; Urinary Bladder Neoplasms; Neuroendocrine Tumors; Mesothelioma; Breast Neoplasms; Prostatic Neoplasms; Oropharyngeal Neoplasms; Genital Neoplasms, Female; Carcinoma, Non-Small-Cell Lung | Details |
Recombinant human annexin 5 protein (Yabao Pharmaceuticals) | SY-005 | Phase 2 Clinical | Lawson Health Research Institute, Yabao Pharmaceutical Group Co Ltd | Sepsis; Coronavirus Infections | Details |
tPA/HisproUK (Thrombolytic Science) | TS-01 | Phase 2 Clinical | Thrombolytic Science | Stroke | Details |
Upamostat Hydrogen Sulphate | WX-671; LH-011; RHB-107 | Phase 1 Clinical | Wilex | Pancreatic Neoplasms; Coronavirus Disease 2019 (COVID-19); Breast Neoplasms | Details |
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