Kollagenase, Typ IV, Pulver
Gibco™

Kollagenase, Typ IV, Pulver

Kollagenase ist eine Protease, die die Bindung zwischen einer neutralen Aminosäure (X) und Glycin in Pro-X-Glyc-Pro aufspaltet, eine Sequenz, dieWeitere Informationen
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KatalognummerMenge
171040191 g
Katalognummer 17104019
Preis (EUR)
538,00
Each
Menge:
1 g
Preis (EUR)
538,00
Each
Kollagenase ist eine Protease, die die Bindung zwischen einer neutralen Aminosäure (X) und Glycin in Pro-X-Glyc-Pro aufspaltet, eine Sequenz, die in hohem Maße in Kollagen zu finden ist. Als einzige Protease ist die Kollagenase in der Lage, die Tripelhelix der nativen Kollagenfibrillen im Bindegewebe, zum Beispiel in der Haut, in Sehnen, Blutgefäßen und Knochen, abzubauen. Diese Eigenschaft der Kollagenase kann für Gewebekulturen aus menschlichen Tumoren, Mausnieren, adultem und fötalem Gehirn oder auch Epithelgewebe genutzt werden. Die Kollagenase wirkt relativ schonend, löst gut bei physiologischem Temperatur- und pH-Wert und erfordert keine spezielle Ausrüstung oder mechanische Einwirkung.

Gibco™ Kollagenase Typ IV wird aus Clostridium histolyticum isoliert und als lyophilisiertes, nicht steriles Pulver für Forschungszwecke bei Zell- oder Gewebedissoziation und Organperfusionen verpackt. Die Aktivität von Gibco™ Kollagenase Typ IV ist für mehr als 160 Einheiten/mg garantiert. Im Vergleich zu anderen Kollagenase-Zubereitungen hat Gibco™ Kollagenase Typ IV eine geringe tryptische Aktivität und eignet sich gut für die Verdauung von Inselzellen aus der Bauchspeicheldrüse.
Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.
Specifications
Menge1 g
Haltbarkeit24 Monate
VersandbedingungRaumtemperatur
FormLyophilisiert
ProdukttypKollagenase
SterilitätUnsteril
Unit SizeEach
Inhalt und Lagerung
Lagerbedingungen: 2 bis 8 °C. Vor Licht schützen.
Versandbedingungen: Haltbarkeit bei
Raumtemperatur: 24 Monate ab Herstellungsdatum

Häufig gestellte Fragen (FAQ)

How do I make the 1000X stock (100 U/µL) solution from Collagenase powder?

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.

Why is collagenase type IV favored over dispase even though the dissociation with collagenase IV seems to take longer (between 30 and 60 min, depending from the lot, at 37 degrees C) compared to dispase?

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.

What reagents do you offer for cell dissociation, and what are the main differences between them?

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.

Zitierungen und Referenzen (3)

Zitierungen und Referenzen
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