Matrixome iMatrix 511 Stem Cell Culture Substrate

Code: NP892-01
  • $344.00
  • (Delivery from $80.00 )
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Recombinant Laminin-511 E8-Fragments

iMatrix-511 is a highly purified and refined laminin-511 E8 fragments, produced in CHO cells.

iMatrix-511 features make it an ideal matrix for pluripotent stem cell culture:

  • Promotes greater stem cell adhesion than all other matrix proteins that have been tested
  • Easy to use (liquid format)
  • E8 fragments retain integrin binding specificity and capacity, and display higher potency than natural Laminin-511
  • Equivalent performance, but lower cost than the legacy iMatrix-511 product

Laminin is localized to the basement membrane, and plays a key role in cell adhesion and proliferation. Laminin-511 (α5, β1 laminin) binds to integrin α6β1 to promote cell signaling. Laminin-511 provides an ideal matrix for the proliferation of a wide variety of cell types including stem and iPS cells.

iMatrix-511 is functionally equivalent to iMatrix-511 SILK (Cat. No. NP892-021). The only difference is the expression system used for bioproduction. The iMatrix-511 SILK product is produced in recombinant silkworm cocoon, while iMatrix-511  is produced in CHO-S cells. Both are E8 fragments that have been purified using the same processes.

Product Name

iMatrix-511 Stem Cell Culture Substrate

Catalog Number




  • NP891-011: 2 × 175 µg
  • NP891-012: 6 × 175 µg

Molecular Weight

150 kDa


>95% pure


Purified Laminin-511 E8 proteolytic fragment

Storage and Stability

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


500 µg/mL


CHO cells

Quality Control

Integrin binding Kd < 10 nM



Notice To Purchaser

REPROCELL is a licensed distributor of Matrixome cell culture substrates to the global market.

Recommended Usage

iMatrix-511 is suitable for use as a substrate for culture of various cell types, including ES/iPS cells.


Matrixome Corporation (Japan)

  1. Takayama K. et al., "Laminin 411 and 511 promote the cholangiocyte differentiation of human induced pluripotent stem cells". Biochemical and Biophysical Research Commun.474 (1): 91-96 (2016).
  2. Nishimura K. et al., "Estradial facilitates functional integration of iPSC-derived dopaminergic neurons into striatal neuronal circuits via activation of integrin a5b1". Stem Cell Reports6  (4): 511-524 (2016).
  3. Matsuno K. et al., "Redefining definitive endoderm subtypes by robust induction of human induced pluripotent stem cells". Differentiation2016.04.002.
  4. Hayashi R. et al., "Co-ordinated ocular development from human iPS cells and recovery of corneal function". Nature531, 368-80 (2016),
  5. Sasaki K. et al., "Robust in vitro induction of human germ cell fate from pluripotent stem cells". Cell Stem Cell 17 (2):178-194 (2015).
  6. Okumura N. et al., "Laminin-511 and -521 enable efficient in vitro expansion of human corneal endothelial cells". Invest Ophthalmal Vis Sci.56 (5), 2933-42 (2015).
  7. Nakagawa M. et al., "A novel efficient feeder-free culture system for the derivation of human induced pluripotent stem cells". Scientific Reports 4: 3594 (2014).
  8. Miyazaki T. et al. "Laminin E8 fragments support efficient adhesion and expansion of dissociated human pluripotent stem cells." Nature Communications 3: 1236 (2012).
  9. 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).
  10. 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).

Additional Publications