Human Cathepsin B

Native whole molecule & biologically active

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+49 (0) 40 . 43 20 84 48 0

 

Product Overview, Sizes and Prices

 

Proteins

Synonyms: CatB, APP secretase, APPS, CTSB

Biological Activity: ≥ 200 units/mg protein

Source: Human Liver

Purity: ≥ 95% by SDS-PAGE

Physical State: Frozen in 50 mM Na Acetate, pH 5.0, with 1 mM EDTA

Manufacturer:  Athens Research & Technology

Article No.SizePrice 
16-12-030102-25UG 25 µg 255 €
16-12-030102-50UG 50 µg 385 €

Please inquire for other vial sizes and custom vialing.

 

 

Produktdetails

Synonyms

CatB, APP secretase, APPS, CTSB

 

Description of Human Cathepsin B

Cathepsin B is a lysosomal cysteine protease synthesized as a 339-amino acid preproenzyme that matures into a heterodimer of 27.5 kDa and 5 kDa subunits linked by disulfide bonds. Its unique occluding loop structure enables dual endopeptidase and exopeptidase activities, preferentially cleaving substrates with hydrophobic or basic residues at pH 4.6 (lysosomal) versus neutral pH 7.2 (cytosolic). Beyond intracellular protein degradation, Cathepsin B modulates lysosomal biogenesis by regulating transcription factor EB (TFEB) and mechanistic target of rapamycin (mTOR) pathways, enhancing autophagy for pathogen clearance. In thyroid epithelial cells, it processes thyroglobulin to liberate thyroxine, requiring TSH-dependent secretion of mature enzyme from lysosomes. Pathologically, Cathepsin B overexpression drives cancer metastasis by degrading extracellular matrix components at tumor invasive fronts, correlating with poor prognosis in breast, lung, and cervical cancers. In Alzheimer’s disease, lysosomal leakage releases Cathepsin B into the cytosol, where it cleaves tau and amyloid precursor protein, exacerbating neurofibrillary tangles and neuronal death. Traumatic brain injury models show Cathepsin B knockout reduces Bax-mediated apoptosis and motor deficits. Rheumatoid arthritis synovial fibroblasts exhibit CTSB-dependent ferroptosis, with inhibition by CA-074Me suppressing lipid ROS accumulation and migration. Therapeutically, pH-selective inhibitors like Z-Arg-Lys-AOMK (IC₅₀ = 20 nM at pH 7.2) target cytosolic Cathepsin B in neurodegeneration while sparing lysosomal function. In breast cancer, dual inhibition of Cathepsin B and Z reduces lung metastasis by 70%, highlighting synergy in protease targeting. Diagnostic applications leverage elevated serum Cathepsin B as a biomarker for sepsis severity (>45 ng/mL), COVID-19 progression, and cardiovascular risk stratification. These multifaceted roles underscore its potential as a therapeutic node across oncology, neurology, and autoimmunity.

 

Source

Prepared from liver shown to be non reactive for HBsAg, anti-HCV, anti-HBc, and negative for anti-HIV 1 & 2 by FDA-required tests.

 

Biological Activity

≥ 200 units/mg protein. One unit is defined as the amount of enzyme that hydrolyzes 1 µmol of Z-Arg-Arg-beta-naphthylamide per minute at 40 °C, using 100 mM Na/K phosphate, pH 6.0, with 1.33 mM EDTA and 2 mM DTT as the activation buffer

 

Storage

For long term, store Human Cathepsin B at ≤ -80°C.

 

Applications

Cancer, Alzheimer's, Brain Injury, Rheumatoid Arthritis, In Vitro Diagnostics.

 

Citations/Publications

Luo, D. et al., (2020), 'Nanoparticles Yield Increased Drug Uptake and Therapeutic Efficacy upon Sequential Near-Infrared Irradiation', ACS Nano, 14: pp 15193−15203. Available at: https://dx.doi.org/10.1021/acsnano.0c05425
Luo, D., et al., (2022), 'Targeted Chemoradiotherapy of Prostate Cancer Using Gold Nanoclusters with Protease Activatable Monomethyl Auristatin E', ACS Appl. Mater. Interfaces, 14: pp 14916−14927. Available at: https://doi.org/10.1021/acsami.1c23780
Kratschmer, C., et al., (2018), 'Targeted Delivery of Auristatin-Modified Toxins to Pancreatic Cancer Using Aptamers', Molecular Therapy: Nucleic Acids., 10: pp 227-236. Available at: https://doi.org/10.1016/j.omtn.2017.11.013
Sanman, L. E., et al., (2016), 'Bifunctional Probes of Cathepsin Protease Activity and pH Reveal Alterations in Endolysosomal pH during Bacterial Infection', Cell Chemical Biology, 23(7): pp 793 - 804. Available at: http://dx.doi.org/10.1016/j.chembiol.2016.05.019
Gbadegesin, O. D., et al., (2025), 'Gemcitabine–Doxorubicin Combination Polymer-Drug Conjugate Prepared by SPAAC Click Chemistry: In Vitro Characterization', Int. J. Mol. Sci., 26: pp 2798. Available at: https://doi.org/10.3390/ijms26062798
NCBI: https://www.ncbi.nlm.nih.gov/protein/P07858/

 

Shipping symbol Shipped with dry ice

 

Gel Scan of Human Cathepsin B

<strong>Fig. 1</strong>: SDS-PAGE Gel

Fig. 1: SDS-PAGE Gel

 

 

 

 

 

 

 

Usage: For research use only. Not for use in diagnostic or therapeutic procedures. Not for human use.

 

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Payment Methods

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Shipping

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