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www.pelobiotech.com<br />
Ask for PD Collagenase!<br />
The products below are defined by the total Wünsch activity per bottle, an assay that uses a peptide substrate to measure<br />
the activity of the collagenase catalytic domain. This activity does not provide functional assessment of collagenase activity<br />
but it is one of the most consistent and reliable activity measures used by many collagenase suppliers. The table below<br />
provides ordering information and a cross reference chart to indicate which PD Collagenase product may meet your needs.<br />
The Collagenase Gold product is similar to the PD Collagenase 800 but does not contain any supplemental purified<br />
protease. This product enables users to use other proteases or to purchase from VC the same protease used in the PD<br />
Collagenase products (BP Protease, catalog # 003-1000) for creation of a custom mixture.<br />
Product Catalog # #/Quantity Cross Reference<br />
PD Collagenase 100<br />
PD Collagenase 800<br />
Collagenase Gold<br />
PB- 011-<br />
1010<br />
PB-011-<br />
1050<br />
PB-011-<br />
1060<br />
1 g<br />
Worthington Type 1 or 2 Liberase TM or DH,<br />
Blendzyme 1 or 2<br />
1 g Liberase TL, Liberase DL, Liberase H I<br />
1 g Human Islets<br />
To isolate sensitive cells such as islets, high purity and fidelity collagenase are essential due to their critical role in enzymatic<br />
degradation of the extracellular matrix without damaging the structural and functional integrity of the cells. Successful<br />
human islet isolation requires the use of defined collagenase-protease enzyme mixtures, and intact class I and class II<br />
collagenase should be used to ensure maximal islet recovery at the lowest dose of enzyme. This is why Collagenase Gold<br />
is ideal for islet isolation. Thereby the use of these enzymes which are GMP and AOF can help with the best results. It has<br />
been found that excess collagenase may potentially harm islets during the isolation process, emphasizing the need for<br />
precise dosing and high purity enzymes to avoid detrimental effects on the isolated cells. Furthermore, studies have<br />
demonstrated that islet mass, quality, and purity are determined by the efficacy of islet isolation, which depends on factors<br />
such as organ procurement, collagenase digestion, and purification method. This highlights the critical role of high purity<br />
collagenase in ensuring the quality and purity of isolated islets.<br />
References<br />
1. Breite AG, et al. Transplantation Proceedings 42 (2010); 2052-2054.<br />
2. McCarthy RC, et al. Transplant Proc 40 (2008); 339-342.<br />
3. Wünsch E and Hedrich H-G. Hoppe-Seyler’s Zeitschrift Physiol Chemie 333 (1963);149-151.<br />
4. Mitchell WM and Harrington WF. Methods in Enzymology (1970) 635-642.<br />
5. McCarthy RC, et al. Transplant 91 (2011) 137-145.<br />
Scan the QR code to visit the VitaCyte website to get additional protocols and product<br />
information.<br />
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