Cell-Vive™ GMP Recombinant Human Cystatin C (carrier-free)

Pricing & Availability
Other Names
Cystatin-3, Gamma-trace, Neuroendocrine basic polypeptide, Post-gamma-globulin, gamma-CSF, post-gamma protein
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Product Citations
publications
CV_GMP_RECOM_Human_Cystatin_C_carrier_free_111824
The activity of human Cystatin C was measured by its ability to inhibit papain activity. The papain activity was monitored by the cleavage of a fluorogenic substrate, Z-FR-AMC, with 50 ng/mL of activated papain. The recombinant human Cystatin C displays a value of IC50 < 6 nM.
  • CV_GMP_RECOM_Human_Cystatin_C_carrier_free_111824
    The activity of human Cystatin C was measured by its ability to inhibit papain activity. The papain activity was monitored by the cleavage of a fluorogenic substrate, Z-FR-AMC, with 50 ng/mL of activated papain. The recombinant human Cystatin C displays a value of IC50 < 6 nM.
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756224 50 µg 840€
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756226 500 µg 3156€
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Description

A member of the the cystatin sub-family, Cystatin C was initially identified in human urine and named gamma-trace. The cystatin family contains three subfamilies: Type 1 cystatins, also known as stefins, which are predominantly present in the cytosol and the nuclei; Type 2 cystatins are mainly secreted proteins; Type 3 cystatins are multi-domain proteins of high molecular weight (60-120 kD) and are also known as kininogens. Cystatin C inhibits cysteine proteases from the papain family and legumain. It forms tight non-covalent associations with its target enzymes. Cystatin C antagonizes TGF-β signaling in normal and cancer cells in vitro. In this process, Cystatin C binds to the TGF-β type II receptor and inhibits the binding of TGF-β. Cystatin C influences the progression of diseases such as, cancer metastasis, atherosclerosis, aortic aneurisms, emphysema, and arthritis. Also, it is associated with neurodegenerative disease and cerebral angiopathy. Human Cystatin C has the tendency to dimerize in order to produce very tight two-fold symmetric dimers. This amyloidogenic property suggests a mechanism for its aggregation in the brain arteries of elderly people with amyloid angiopathy. The L68Q mutant of human Cystatin C is responsible for conformational disease, which causes massive amyloidosis, cerebral hemorrhage, and death in young adults.

Product Details
Quality Statement

BioLegend Cell-Vive™ GMP Recombinant proteins are manufactured and tested in accordance with USP Chapter 1043, Ancillary Materials for Cell, Gene and Tissue-Engineered Products and Ph. Eur. Chapter 5.2.12 in a dedicated GMP facility compliant with ISO 13485:2016. Specifications and processes include:

  • Low endotoxin level (≤ 0.1 EU/μg)
  • Purity (≥ 95% or higher)
  • Bioburden testing
  • Mycoplasma testing
  • Batch-to-batch consistency
  • Vendor qualification
  • Raw material traceability and documentation
  • Documented procedures and employee training
  • Equipment maintenance and monitoring records
  • Lot-specific certificates of analysis
  • Quality audits per ISO 13485:2016
  • QA review of released products
Technical data sheet

Product Details

Source
Human Cystatin C, amino acids Ser27-Ala146 (Accession# P01034) was expressed in 293E cells. The carboxy-terminal contains a TG-10His-GGQtag.
Molecular Mass
The 135 amino acid recombinant protein has a predicted molecular mass of 15.1 kD. The non-reduced and DTT-reduced protein migrates at approximately 17 kD by SDS-PAGE. The predicted N-terminal amino acid is Serine.
N-terminal
Sequence Analysis
Ser-Ser-Pro-Gly-Lys-Pro-Pro-Arg-Leu-Val
Purity
≥ 95%, as determined by Coomassie stained SDS-PAGE
Formulation
Protein was lyophilized from 0.1 μm filtered solution containing 20mM HEPES, 0.1M NaCl, pH7.2
Endotoxin Level
Less than or equal to 0.1 EU per μg of protein as determined by LAL method.
Residual Host Cell Protein Content
≤ 0.50 ng/μg by ELISA
Concentration
50 μg and 500 μg sizes are lyophilized
Storage & Handling
Unopened vial can be stored between 2°C and 8°C for up to 2 weeks, at - 20°C or colder until the expiration date. Reconstitute lyophilized protein in sterile water. Before reconstitution, make sure sterile water and product are at room temperature. Quickly spin the vial or gently tap down on the vial to make sure the lyophilized product is at the bottom of the vial before opening. Use aseptic techniques to add the required volume of reconstitution buffer (sterile water) to the vial, to obtain the recommended stock concentration 250 μg/mL. Close the vial and leave at ambient temperature for 15-20 minutes. Then gently invert the vial several times or until all of the lyophilized product dissolves. Leave the vial at room temperature for another 15 minutes. If small particulates are still observed after 15 minutes, incubate at room temperature for an additional 30 minutes and leave the vial at 2°C - 8°C overnight. Next day, invert the vial several times or gently pipette the solution up and down before use. If needed, transfer the reconstituted stock solution to a sterile container for additional dilution to no less than 100 μg/mL. Small working aliquots in polypropylene tubes can be made after reconstitution and store the vials at -20°C or lower. Avoid freeze/ thaw cycles. Carrier protein such as 0.2 - 1% endotoxin-free BSA or HSA can be added when preparing the stock solution. Aliquots can be stored between 2°C and 8°C for up to two weeks or stored at -20°C or colder for up to 3 months.
Activity
IC50 < 6.0 nM, as determined by inhibiting human Papain (0.05 μg/mL) activity when 100 µM of Z-FR-AMC is used as a papain peptide substrate.
Application

Bioassay

Application Notes

Our lyophilized proteins are validated in-house to maintain activity after shipping at ambient temperature and are backed by our 100% satisfaction guarantee. If you have any concerns, contact us at tech@biolegend.com.

Disclaimer

BioLegend Cell-Vive™ GMP Recombinant proteins are for research use only. Suitable for ex vivo cell processing. Not for injection or diagnostic or therapeutic use. Not for resale. BioLegend will not be held responsible for patent infringement or other violations that may occur with the use of our products.

Antigen Details

Structure
Monomer
Function
Inhibitor of cysteine proteases (capthepsins B, H, K, L, and S). Transcription factor IFN regulatory factor 8 (IRF-8) induces cystatin C in mouse primary dendritic cells. IL-10 inhibits IRF-8 and consequently Cystatin C.
Interaction
Normal and cancer cells.
Ligand/Receptor
Papain-like cysteine proteases, cathepsins B, H, K, L, and S, and legumain.
Bioactivity
Cystatin C inhibits the activity of papain.
Cell Sources
Considered ubiquitously expressed, biological fluids, dendritic cells, and macrophages.
Antigen References
  1. Grubb A, et al. 1982. Proc. Nat. Acad. Sci. 79:3024.
  2. Janowski R, et al. 2001. Nat. Struct. Biol. 8:316.
  3. Sokol JP, Schiemann WP. 2004. Mol. Cancer Res. 2:183.
  4. Bird PI, et al. 2009. Nat Rev Immunol. 9:871.
  5. Kaur G, Levy E. 2012. Front Mol. Neurosci. 5:79.
  6. Xu Y, et al. 2014. J Biol Chem. 289:9730.
  7. Xu Y, et al. 2015. Immunol. Cell Biol. 5:442.
Gene ID
1471 View all products for this Gene ID
UniProt
View information about Cystatin C on UniProt.org

Related FAQs

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Go To Top Version: 1    Revision Date: 12.04.2024

For Research Use Only. Suitable for ex vivo cell processing. Not for injection or diagnostic or therapeutic use.

 

This product is supplied subject to the terms and conditions, including the limited license, located at www.biolegend.com/terms ("Terms") and may be used only as provided in the Terms. Without limiting the foregoing, BioLegend products may not be used for any Commercial Purpose as defined in the Terms, resold in any form, used in manufacturing, or reverse engineered, sequenced, or otherwise studied or used to learn its design or composition without express written approval of BioLegend. Regardless of the information given in this document, user is solely responsible for determining any license requirements necessary for user’s intended use and assumes all risk and liability arising from use of the product. BioLegend is not responsible for patent infringement or any other risks or liabilities whatsoever resulting from the use of its products.

 

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