Dispase II, powder
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Dispase II, powder
Gibco™

Dispase II, powder

ディスパーゼII(中性プロテアーゼ)は、非極性アミノ酸残基のN末端ペプチド結合を加水分解するアミノエンドペプチダーゼです。この配列はコラーゲン内で高い頻度で検出されます。ディスパーゼIIには穏やかなタンパク質分解作用があり、初代細胞の分離やルーチンの継代に有用です。ディスパーゼIIは比較的穏やかで、生理学的温度とpHで良好に解離し、一般的に細胞膜の完全性を維持します詳細を見る
製品番号(カタログ番号)数量
171050415 g
製品番号(カタログ番号) 17105041
価格(JPY)
21,000
Each
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数量:
5 g
ディスパーゼII(中性プロテアーゼ)は、非極性アミノ酸残基のN末端ペプチド結合を加水分解するアミノエンドペプチダーゼです。この配列はコラーゲン内で高い頻度で検出されます。ディスパーゼIIには穏やかなタンパク質分解作用があり、初代細胞の分離やルーチンの継代に有用です。ディスパーゼIIは比較的穏やかで、生理学的温度とpHで良好に解離し、一般的に細胞膜の完全性を維持します。

Gibco™ディスパーゼIIは、バシラスポリミキサで製造され、細胞または組織の解離における研究用に凍結乾燥された未滅菌粉末として包装されていて、浮遊培養の凝集を防止します。Gibco™ディスパーゼIIの活性は、0.5ユニット/mgを超えることが保証されています
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5 g
品質保持期間24 Months
出荷条件Room Temperature
形状Lyophilized
製品タイプCell Culture Dissociation Reagent
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)

What is the stability of reconstituted Dispase?

The Dispase solution is stable at -5 to -20 degrees C for a minimum of 1 month.

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

I have Dispase, Cat. No. 17105041. Is it Dispase I or II?

This product is Dispase II.

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 (2)

引用および参考文献
Abstract
Isolation, cultivation and characterization of adult murine prostate stem cells.
Authors:Lukacs RU, Goldstein AS, Lawson DA, Cheng D, Witte ON,
Journal:Nat Protoc
PubMed ID:20360765
'The successful isolation and cultivation of prostate stem cells will allow us to study their unique biological properties and their application in therapeutic approaches. Here we describe step-by-step procedures on the basis of previous work in our laboratory for the harvesting of primary prostate cells from adolescent male mice by ... 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