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Recombinant Human TIMP-1 Protein, CF

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Summary
Reactivity HuSpecies Glossary
Applications Inhibition Activity
Format
Carrier-Free

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Recombinant Human TIMP-1 Protein, CF Summary

Details of Functionality
Measured by its ability to inhibit human MMP-2 cleavage of a fluorogenic peptide substrate Mca-PLGL-Dpa-AR-NH2 (Catalog # ES001). The IC50 value is approximately 2.5 nM as measured under the described conditions. 
Source
Mouse myeloma cell line, NS0-derived human TIMP-1 protein
Cys24-Ala207
Accession #
N-terminal Sequence
Cys24
Protein/Peptide Type
Recombinant Enzymes
Gene
TIMP1
Purity
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain
Endotoxin Note
<1.0 EU per 1 μg of the protein by the LAL method.

Applications/Dilutions

Dilutions
  • Inhibition Activity
Theoretical MW
21 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.
SDS-PAGE
28-30 kDa, reducing conditions
Publications
Read Publications using
970-TM in the following applications:

Packaging, Storage & Formulations

Storage
Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
  • 6 months from date of receipt, -20 to -70 °C as supplied.
  • 3 months, -20 to -70 °C under sterile conditions after reconstitution.
Buffer
Lyophilized from a 0.2 μm filtered solution in Sodium Acetate and NaCl.
Purity
>95%, by SDS-PAGE under reducing conditions and visualized by silver stain
Reconstitution Instructions
Reconstitute at 100 μg/mL in sterile, deionized water.
Assay Procedure
  • Assay Buffer: 50 mM Tris, 10 mM CaCl2, 150 mM NaCl, 0.05% Brij-35 (w/v), pH 7.5 (TCNB)
  • Recombinant Human TIMP-1 (rhTIMP-1) (Catalog # 970-TM)
  • Recombinant Human MMP‑2 (rhMMP‑2) (Catalog # 902-MP)
  • p-aminophenylmercuric acetate (APMA), (Sigma, Catalog # A-9563), 100 mM stock in DMSO
  • Substrate: MCA-Pro-Leu-Gly-Leu-DPA-Ala-Arg-NH2 (Catalog # ES001), 2 mM stock in DMSO
  • F16 Black Maxisorp Plate (Nunc, Catalog # 475515)
  • Fluorescent Plate Reader (Model: SpectraMax Gemini EM by Molecular Devices) or equivalent
  1. Activate rhMMP-2 at 100 µg/mL with 1 mM of APMA at final concentration respectively, in Assay Buffer.
  2. Incubate activation of rhMMP-2 at 37°C for 1 hour.
  3. Prepare a curve of rhTIMP-1 (MW: 20,695 Da). Make the following serial dilutions in Assay Buffer: 2000 nM, 1,000 nM, 500 nM, 300 nM, 200 nM, 150 nM, 100 nM, 20 nM, and 2 nM.
  4. Dilute activated 100 µg/mL rhMMP-2 to 12.8 µg/mL in Assay Buffer.
  5. Mix 25 µL of 12.8 µg/mL rhMMP-2, 16 µL of rhTIMP-1 serial curve dilutions, and 119 µL of Assay Buffer in micro-tubes.
  6. Include two enzyme controls of 25 µL of 12.8 µg/mL rhMMP-2 and 135 mL Assay Buffer in micro-tubes.
  7. Incubate reaction mixtures at 37 °C for 2 hours.
  8. Dilute incubated reaction mixtures by a 5-fold dilution in Assay Buffer.
  9. Dilute Substrate to 10 µM in Assay Buffer.
  10. In a plate load 50 µL of 5-fold diluted incubated reaction mixtures to wells.
  11. Start the reaction by adding 50 µL of 10 µM Substrate to wells.
  12. Read at excitation and emission wavelengths of 320 nm and 405 nm (top read), respectively in kinetic mode for 5 minutes.
  13. Derive the IC50 value of rhTIMP-1 from the curve.
  14. Calculate specific activity for each point using the following formula (if needed):

     Specific Activity (pmol/min/µg) =

Adjusted Vmax* (RFU/min) x Conversion Factor** (pmol/RFU)
amount of enzyme (µg)

     *Adjusted for Substrate Blank

     **Derived using calibration standard MCA-Pro-Leu-OH (Bachem, Catalog # M-1975).

Per Well:
  • rhMMP-2: 0.02 µg
  • rhTIMP-1 curve: 20 nM, 10 nM, 5 nM, 3 nM, 2 nM, 1.5 nM, 1.0 nM, 0.2 nM, 0.02 nM, and 0 nM
  • Substrate: 5 µM

Notes

This product is produced by and ships from R&D Systems, Inc., a Bio-Techne brand.

Alternate Names for Recombinant Human TIMP-1 Protein, CF

  • CLGI
  • Collagenase inhibitor
  • collagenase inhibitor)
  • EPATIMP-1
  • EPO
  • erythroid potentiating activity
  • Erythroid-potentiating activity
  • Fibroblast collagenase inhibitor
  • FLJ90373
  • HCI
  • metalloproteinase inhibitor 1
  • TIMP metallopeptidase inhibitor 1
  • TIMP1
  • TIMP-1
  • TIMPtissue inhibitor of metalloproteinase 1 (erythroid potentiating activity
  • Tissue inhibitor of metalloproteinases 1

Background

Tissue inhibitors of metalloproteinases or TIMPs are a family of proteins that regulate the activation and proteolytic activity of the zinc enzymes known as matrix metalloproteinases (MMPs). There are four members of the family, TIMP-1, TIMP-2, TIMP-3 and TIMP-4. TIMP-1 is a glycoprotein with a molecular mass of 28 kDa produced by a wide range of cell types. TIMP-1 inhibits active MMP-mediated proteolysis by forming an N-terminal, non-covalent binary complex with the MMP active site. TIMP-1 also associates C-terminally with Pro-MMP-9 in a complex which may play a role in regulating activation. Independent of MMPs, TIMP-1 has been shown to have a role in tissue homeostasis.

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Publications for TIMP-1 (970-TM)(19)

We have publications tested in 5 confirmed species: Human, Mouse, Rat, N/A, Primate - Chlorocebus pygerythrus (Vervet Monkey).

We have publications tested in 8 applications: Bioassay, ELISA (Standard), ELISA Standard, Enzyme Activity, Enzyme Assay, Enzyme Inhibition, In Vivo, Tissue Culture.


Filter By Application
Bioassay
(11)
ELISA (Standard)
(1)
ELISA Standard
(1)
Enzyme Activity
(1)
Enzyme Assay
(1)
Enzyme Inhibition
(1)
In Vivo
(1)
Tissue Culture
(1)
All Applications
Filter By Species
Human
(9)
Mouse
(5)
Rat
(1)
N/A
(2)
Primate - Chlorocebus pygerythrus (Vervet Monkey)
(1)
All Species
Showing Publications 1 - 10 of 19. Show All 19 Publications.
Publications using 970-TM Applications Species
A Minns, Y Qi, K Yamamoto, K Lee, J Ahnström, S Santamaria The C-terminal domains of ADAMTS1 contain exosites involved in its proteoglycanase activity The Journal of Biological Chemistry, 2023-02-21;0(0):103048. 2023-02-21 [PMID: 36813235] (Bioassay, N/A) Bioassay N/A
SK Chintala, J Pan, S Satapathy, R Condruti, Z Hao, PW Liu, CF O'Conner, JT Barr, MR Wilson, S Jeong, ME Fini Recombinant Human Clusterin Seals Damage to the Ocular Surface Barrier in a Mouse Model of Ophthalmic Preservative-Induced Epitheliopathy International Journal of Molecular Sciences, 2023-01-04;24(2):. 2023-01-04 [PMID: 36674497] (In Vivo, Mouse) In Vivo Mouse
QC Larrouture, AP Cribbs, SR Rao, M Philpott, SJ Snelling, HJ Knowles Loss of mutual protection between human osteoclasts and chondrocytes in damaged joints initiates osteoclast-mediated cartilage degradation by MMPs Scientific Reports, 2021-11-22;11(1):22708. 2021-11-22 [PMID: 34811438] (Bioassay, Human) Bioassay Human
S Santamaria, DR Martin, X Dong, K Yamamoto, SS Apte, J Ahnström Post-Translational Regulation And Proteolytic Activity Of The Metalloproteinase Adamts8 The Journal of Biological Chemistry, 2021-10-21;0(0):101323. 2021-10-21 [PMID: 34687701] (Enzyme Activity, Human) Enzyme Activity Human
U Mirastschi, B Lupše, K Maedler, B Sarma, A Radtke, G Belge, M Dorsch, D Wedekind, LJ McCawley, G Boehm, U Zier, K Yamamoto, S Kelm, MS Ågren Matrix Metalloproteinase-3 is Key Effector of TNF-alpha-Induced Collagen Degradation in Skin Int J Mol Sci, 2019-10-22;20(20):. 2019-10-22 [PMID: 31652545] (Bioassay, Mouse) Bioassay Mouse
JD Kumar, I Aolymat, L Tiszlavicz, Z Reisz, HM Garalla, R Beynon, D Simpson, GJ Dockray, A Varro Chemerin acts via CMKLR1 and GPR1 to stimulate migration and invasion of gastric cancer cells: putative role of decreased TIMP-1 and TIMP-2 Oncotarget, 2019-01-04;10(2):98-112. 2019-01-04 [PMID: 30719206] (Bioassay, Human) Bioassay Human
KK Wong, F Zhu, I Khatri, Q Huo, DE Spaner, RM Gorczynski Characterization of CD200 Ectodomain Shedding PLoS ONE, 2016-04-25;11(4):e0152073. 2016-04-25 [PMID: 27111430] (Bioassay, Human) Bioassay Human
Uchikawa S, Yoda M, Tohmonda T, Kanaji A, Matsumoto M, Toyama Y, Horiuchi K ADAM17 regulates IL-1 signaling by selectively releasing IL-1 receptor type 2 from the cell surface. Cytokine, 2014-11-22;71(2):238-45. 2014-11-22 [PMID: 25461404] (Bioassay, Primate - Chlorocebus pygerythrus (Vervet Monkey)) Bioassay Primate - Chlorocebus pygerythrus (Vervet Monkey)
Agren M, Schnabel R, Christensen L, Mirastschijski U Tumor necrosis factor-alpha-accelerated degradation of type I collagen in human skin is associated with elevated matrix metalloproteinase (MMP)-1 and MMP-3 ex vivo. Eur J Cell Biol, 2014-10-23;94(1):12-21. 2014-10-23 [PMID: 25457675] (Tissue Culture, Human) Tissue Culture Human
Vandooren J, Born B, Solomonov I, Zajac E, Saldova R, Senske M, Ugarte-Berzal E, Martens E, Van den Steen P, Van Damme J, Garcia-Pardo A, Froeyen M, Deryugina E, Quigley J, Moestrup S, Rudd P, Sagi I, Opdenakker G Circular trimers of gelatinase B/matrix metalloproteinase-9 constitute a distinct population of functional enzyme molecules differentially regulated by tissue inhibitor of metalloproteinases-1. Biochem J, 2015-01-15;465(2):259-70. 2015-01-15 [PMID: 25360794] (Bioassay, Mouse) Bioassay Mouse
Show All 19 Publications.

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Bioinformatics

Gene Symbol TIMP1
Uniprot