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Collagen Mimetic peptides MAPTRIX-C-TAIPSCPEGTVPLYS

animal-free ECM peptides, solution, 0.5 mg/mL protein, suitable for cell culture

Sinônimo(s):

MAPTrix™ Technology

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Sobre este item

UNSPSC Code:
12352202
NACRES:
NA.75
Form:
aqueous solution
Technique(s):
cell culture | mammalian: suitable
Concentration:
0.5 mg/mL protein
Mol wt:
~24.1 kDa

Nome do produto

MAPTRIX-C-TAIPSCPEGTVPLYS, Collagen Mimetic, aqueous solution

sterility

Filtered sterilized solution

form

aqueous solution

mol wt

~24.1 kDa

packaging

pkg of 2.5 mg

concentration

0.5 mg/mL protein

technique(s)

cell culture | mammalian: suitable

binding specificity

Domain: α3(IV) NC1
Binding Motif: TAIPSCPEGTVPLYS

shipped in

ambient

storage temp.

2-8°C

Application

MAPTrix™ Technology provides a true extracellular microenvironment (ECM) by presenting combinatorial peptide motifs. The ECM, defined by biochemical cues and physical cues, is a deciding factor in a wide range of cellular processes including cell adhesion, proliferation, differentiation, and expression of phenotype-specific functions.Currently existing technology offers simple and merely adequate environments that facilitate simple cell processes such as cellular adhesion.[1][2] The simple presentation of cell adhesion motifs is not optimal for controlling more integrated processes. Crosstalk among signaling pathways act synergistically to enhance cellular responses such as cell adhesion or proliferation.[3] A study showed that a combination of extracellular matrix derived peptides presented on a surface may enhance cell adhesion strength and focal adhesion assembly. The combinatorial presentation of ECM peptides on cell growth surfaces may also promote elevated proliferation rates of primary or stem cells.[4][5][6]

Features and Benefits

  • Biochemically-defined, animal-free cell culture surfaces designed to enhance cell performance
  • MAPTrix™ produces a uniform ECM surface that provides a highly controlled 2D extracellular microenvironment for cell cultures and related applications
  • Adhesion properties of the mussel adhesive protein makes the coating reproducible & reliable

Legal Information

MAPTrix is a trademark of Kollodis Biosciences

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Sigma-Aldrich

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sterility

Filtered sterilized solution

sterility

Filtered sterilized solution

sterility

Filtered sterilized solution

sterility

Filtered sterilized solution

technique(s)

cell culture | mammalian: suitable

technique(s)

cell culture | mammalian: suitable

technique(s)

cell culture | mammalian: suitable

technique(s)

cell culture | mammalian: suitable

concentration

0.5 mg/mL protein

concentration

0.5 mg/mL protein

concentration

0.5 mg/mL protein

concentration

0.5 mg/mL protein

mol wt

~24.1 kDa

mol wt

~24.2 kDa

mol wt

~24.1 kDa

mol wt

~24.1 kDa

form

aqueous solution

form

aqueous solution

form

aqueous solution

form

aqueous solution

packaging

pkg of 2.5 mg

packaging

pkg of 2.5 mg

packaging

pkg of 2.5 mg

packaging

pkg of 2.5 mg

flash_point_f

Not applicable

flash_point_c

Not applicable

Classe de armazenamento

12 - Non Combustible Liquids

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Certificados de análise (COA)

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S J Fashena et al.
Nature cell biology, 2(12), E225-E229 (2001-01-09)
Over the past twenty years, intensive research has enabled us to identify components of specific signalling pathways downstream of an array of adhesion and growth-factor receptors. The first Gordon Research Conference on 'Signalling by Adhesion Receptors', which took place in
Samuel Schmidt et al.
Cell and tissue research, 339(1), 83-92 (2009-11-19)
Adhesion and migration are integrated cell functions that build, maintain and remodel the multicellular organism. In migrating cells, integrins are the main transmembrane receptors that provide dynamic interactions between extracellular ligands and actin cytoskeleton and signalling machineries. In parallel to
Seung Tae Lee et al.
Biomaterials, 31(6), 1219-1226 (2009-11-21)
We present development and use of a 3D synthetic extracellular matrix (ECM) analog with integrin-specific adhesion ligands to characterize the microenvironmental influences in embryonic stem cell (ESC) self-renewal. Transcriptional analysis of 24 integrin subunits followed by confirmation at the translational
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SKUGTIN
166312K-2.5MG04061838748898

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