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

Collagenase, Type IV, powder

コラゲナーゼは、コラーゲン内で高い頻度で検出されるPro-X-Glyc-Pro配列中の中性アミノ酸(X)とグリシン間の結合を切断するプロテアーゼです。コラゲナーゼは、皮膚、腱腱、血管、骨などの結合組織で一般的に見られる三重らせん天然コラーゲン原線維を分解できる点でプロテアーゼの中で特異的です。コラゲナーゼ分解は詳細を見る
製品番号(カタログ番号)数量
171040191 g
製品番号(カタログ番号) 17104019
価格(JPY)
54,500
Each
お問い合わせください ›
数量:
1 g
コラゲナーゼは、コラーゲン内で高い頻度で検出されるPro-X-Glyc-Pro配列中の中性アミノ酸(X)とグリシン間の結合を切断するプロテアーゼです。コラゲナーゼは、皮膚、腱腱、血管、骨などの結合組織で一般的に見られる三重らせん天然コラーゲン原線維を分解できる点でプロテアーゼの中で特異的です。コラゲナーゼ分解は、ヒト腫瘍、マウス腎臓、ヒトの成人および胎児の脳、および上皮を含む多くの他の組織の培養に適しています。コラゲナーゼは比較的穏やかで、生理学的温度とpHで良好に解離し、機械的撹拌や特別な装置は必要ありません。

Gibco™コラゲナーゼIV型は、ヒストリチクム菌から分離され、細胞または組織の解離および器官灌流における研究用の凍結乾燥非滅菌粉末としてパッケージされています。Gibco™コラゲナーゼIV型の活性は、160ユニット/mgを超えることが保証されていますGibco™コラゲナーゼIV型は、他のコラゲナーゼ製剤と比較してトリプシン活性が低く、膵臓の島細胞の消化に適しています。
研究用にのみ使用できます。診断用には使用いただけません。
仕様
数量1 g
品質保持期間24 Months
出荷条件Room Temperature
形状Lyophilized
製品タイプCollagenase
無菌性Non-sterile
Unit SizeEach
組成および保存条件
Storage conditions: 2°C to 8°C. Protect from light.
Shipping conditions: Room temperature
Shelf life: 24 months from date of manufacture

よくあるご質問(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.

引用および参考文献 (3)

引用および参考文献
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