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Collagenase, Type IV, powder
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Collagenase, Type IV, powder
Gibco™

Collagenase, Type IV, powder

Collagenase is a protease that cleaves the bond between a neutral amino acid (X) and glycine in the sequence Pro-X-Glyc-Pro,Read more
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Catalog NumberQuantity
171040191 g
Catalog number 17104019
Price (USD)
387.00
Each
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Quantity:
1 g
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Price (USD)
387.00
Each
Add to cart
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Collagenase is a protease that cleaves the bond between a neutral amino acid (X) and glycine in the sequence Pro-X-Glyc-Pro, which is found with high frequency in collagen. Collagenase is unique among proteases in its ability to degrade the triple-helical native collagen fibrils commonly found in connective tissues such as skin, tendon, blood vessels, and bone. Collagenase disaggregation is suitable for the culture of human tumors, mouse kidney, human adult and fetal brain, and many other tissues including epithelium. Collagenase is relatively gentle, dissociates well at physiological temperature and pH, and requires no mechanical agitation or special equipment.

Gibco™ Collagenase Type IV is isolated from Clostridium histolyticum and packaged as a lyophilized, non-sterile powder for research use in cell or tissue dissociation and organ perfusions. Gibco™ Collagenase Type IV activity is guaranteed to be greater than 160 units/mg. Compared to other collagenase preparations, Gibco™ Collagenase Type IV has low tryptic activity and is well-suited for the digestion of islet cells from the pancreas.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
Quantity1 g
Shelf Life24 Months
Shipping ConditionRoom Temperature
FormLyophilized
Product TypeCollagenase
SterilityNon-sterile
Unit SizeEach
Contents & Storage
Storage conditions: 2°C to 8°C. Protect from light.
Shipping conditions: Room temperature
Shelf life: 24 months from date of manufacture
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Certificates

Lot #Certificate TypeDateCatalog Number(s)
3185160Certificate of AnalysisJun 18, 202517104019
3124586Certificate of AnalysisMay 30, 202517104019
3124585Certificate of AnalysisMay 04, 202517104019
3124584Certificate of AnalysisApr 06, 202517104019
3093186Certificate of AnalysisFeb 12, 202517104019
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Scientific Resources

Product Information

Frequently asked questions (FAQs)

1. Add 1 mL Hanks' Balanced Salt Solution (HBSS) with calcium and magnesium directly to 1 g vial of Collagenase. Vortex gently to ensure complete dissolution. Transfer to a clean tube.
2. Determine volume of HBSS (with calcium and magnesium) required to bring collagenase solution to 100 U/µL (1000X stock solution). The activity is lot- specific. Rinse vial with this volume of HBSS (with calcium and magnesium), and combine. Filter sterilize 1000X stock solution with a low protein binding filtration unit.
Example: Assuming the lot you have purchased has an activity of 265 U/mg, this lot will have 265000 Units per mL when you reconstitute collagenase into HBSS (with calcium and magnesium) at 1 g/mL. In order to dilute 265000 U/L to 100000 U/mL (= 100 U/µL), you need to dilute the 1 g/mL enzyme solution 2.65 fold.

Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.

Actually, in a feeder-based culture, dispase (2 mg/mL) should take about 15-25 min to work at 37 degrees C. Two to three minutes' dissociation time would apply to feeder-free cultures. Dispase is a more aggressive enzyme, so it works faster, but that also means that when the PSC clumps are harvested, they are more sensitive to being broken apart by trituration. Once the clumps are harvested, they should be pipetted up and down a few times to break up the clumps to the appropriate size. If the cells are harvested with collagenase type IV, they have to be pipetted more times because the clumps are harder to break up, but this means that there is less likelihood to break up the clumps into pieces that are too small. If the cells are harvested with dispase, they have to be pipetted fewer times, and care has to be taken to ensure that the clumps are not broken too much. Either enzyme is fine to use, and if you have enough experience, you may prefer to use dispase to save time. But for a less experienced user, we recommend using collagenase type IV as it is safer and you are less likely to ruin your culture by over-triturating.

Find additional tips, troubleshooting help, and resources within our Cell Culture Support Center.

Please use this selection chart that compares our cell dissociation reagents (https://www.thermofisher.com/us/en/home/life-science/cell-culture/mammalian-cell-culture/reagents/trypsin.html).

Find additional tips, troubleshooting help, and resources within ourMammalian Cell Culture Basics Support Center.

Citations & References (3)

Citations & References
Abstract
Isolation and in vitro culture of primary cardiomyocytes from adult zebrafish hearts.
Authors:Sander V, Suñe G, Jopling C, Morera C, Izpisua Belmonte JC,
Journal:Nat Protoc
PubMed ID:23538883
'This protocol describes how to isolate primary cardiomyocytes from adult zebrafish hearts and culture them for up to 4 weeks, thereby using them as an alternative to in vivo experiments. After collagenase digestion of the ventricle, cells are exposed to increasing calcium concentrations in order to obtain high-purity cardiomyocytes. The ... More
Production of hepatocyte-like cells from human pluripotent stem cells.
Authors:Hannan NR, Segeritz CP, Touboul T, Vallier L,
Journal:Nat Protoc
PubMed ID:23424751
Large-scale production of hepatocytes from a variety of genetic backgrounds would be beneficial for drug screening and to provide a source of cells to be used as a substitute for liver transplantation. However, fully functional primary hepatocytes remain difficult to expand in vitro, and circumventing this problem by using an ... More
Feeder layer- and serum-free culture of human embryonic stem cells.
Authors:Amit M, Shariki C, Margulets V, Itskovitz-Eldor J,
Journal:Biol Reprod
PubMed ID:14627547
In addition to their contribution to the research on early human development, human embryonic stem (hES) cells may also be used for cell-based therapies. Traditionally, these cells have been cultured on mouse embryonic fibroblast feeder layers, which allow their continuous growth in an undifferentiated state. However, the use of hES ... More
3 total citations

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