iMatrix-221 Cardiac and Myoblast Cell Culture Substrate

iMatrix-221's features make it an ideal matrix for some cell culture applications:

• Xeno-free formulation / CHO-S cell bioproduction
• Easy to use (liquid format)
• E8-fragments retain integrin binding specificity and capacity, and display higher potency than natural Laminin-221

iMatrix-221 is a highly purified and refined product of human recombinant laminin-221 (E8 fragment) expressed by CHO-S cells. Laminin-221 is found predominantly in the basal lamina of striated muscle tissues. Expression deficiencies are implicated in muscular dystophy and cardiomyopathies.¹

Laminins of the α-2 type are also a predomiant form found in the human adult heart tissue.² Cultivation of iPSC-drived cardiomyocytes on iMatrix-221 has been demonstrated to maintain strong contractility in attached monolayer culture.³

Matrixome company name and logo and iMatrix brand name are the property of Matrixome Corp., Japan.

Product Name: iMatrix-221 Cardiac and Myoblast Cell Culture Substrate

Catalog Numbers:

• NP892-061
• NP892-062

Sizes:

• NP892-061 — 2 × 175 µg
• NP892-062 — 6 × 175 µg

Molecular Weight: 150 kDa

Purity: > 95 % pure

Formulation: Purified Laminin-221 E8 proteolytic fragment

Storage and Stability: Store at 4 °C and protect from light exposure. Stable for 2 years from manufacturing date.

Quality Control: Activity: K_d for integrin binding

Sterility: Sterile

Notice To Purchaser: REPROCELL is a licensed distributor of Matrixome cell culture substrates to the global market.

Recommended Usage: iMatrix-221 is suitable for use as a substrate for culture of various myoblast cell types, but most notably for cardiomyocytes.

Concentration: 500 µg/mL

Source: CHO-S cell expression

Manufacturer: Matrixome Corporation (Japan)

Safety Data Sheets:

• NP892-06 Safety Data Sheet

Product Flyer:

• iMatrix™ Cell Culture Substrates

1. Oliviero P. et.al., Expression of laminin α2 chain during normal and pathological growth of myocardium in rat and human. Cardiovascular Research 46, 346-355 (2000).
2. Ja K.P. Myu Mia et.al., PSC-derived human cardiac progenitor cells improve ventricular remodeling via angiogenesis and interstitial networking of infarcted myocardium. J Cell Mol Med 20(2), 323-332 (2016).
3. Unpublished, Osaka University (2018).
4. Miyazaki T. et al. Laminin E8 fragments support efficient adhesion and expansion of dissociated human pluripotent stem cells. Nature Communications 3: 1236 (2012).
5. Taniguchi Y. et al., The C-terminal region of laminin β-chains modulates the integrin-binding affinities of laminins. J. Biol. Chem.284 (12): 7820-31 (2009).
6. Ido H. et al., The requirement of the glutamic acid residue at the third position from the carboxyl termini of the laminin gamma-chains in integrin-binding by laminins. J. Biol. Chem. 282 (15): 11144-54 (2017).