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Merck

P3886

Sigma-Aldrich

Poly-L-proline

suitable for ligand binding assays, Mol wt >30,000

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About This Item

Fórmula empírica (notación de Hill):
C5H9NO2
Número de CAS:
Peso molecular:
115.13
MDL number:
UNSPSC Code:
12352209
PubChem Substance ID:
NACRES:
NA.26

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product name

Poly-L-proline, mol wt >30,000

form

powder

mol wt

>30,000

technique(s)

ligand binding assay: suitable

color

white to light yellow

storage temp.

−20°C

SMILES string

OC(=O)C1CCCN1

InChI

1S/C5H9NO2/c7-5(8)4-2-1-3-6-4/h4,6H,1-3H2,(H,7,8)

InChI key

ONIBWKKTOPOVIA-UHFFFAOYSA-N

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Este artículo
GE17-5318-01GE17-0921-07GE17-5318-06
matrix

6% cross-linked agarose

matrix

6% cross-linked agarose

matrix

6% cross-linked agarose

matrix

6% cross-linked agarose

capacity

~40 mg binding capacity (histidine-tagged protein/ml medium when changed with Ni2+)(Protein- and metal-ion dependent.)

capacity

~40 mg binding capacity(histidine-tagged protein)

capacity

~40 mg binding capacity (histidine-tagged protein/ml medium when changed with Ni2+)(Protein- and metal-ion dependent.)

capacity

~40 mg binding capacity(histidine-tagged protein)

packaging

pack of 100 mL

packaging

pack of 25 mL

packaging

pack of 25 mL

packaging

pack of 5 mL

manufacturer/tradename

Cytiva 17-0921-08

manufacturer/tradename

Cytiva 17-5318-01

manufacturer/tradename

Cytiva 17-0921-07

manufacturer/tradename

Cytiva 17-5318-06

average diameter

90 μm

average diameter

90 μm

average diameter

90 μm

average diameter

90 μm

Analysis Note

Molecular weight based on viscosity.

Other Notes

For additional technical information on polyamino acids please visit the Polyamino acid FAQ resource.

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)


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    Helena Bysell et al.
    Langmuir : the ACS journal of surfaces and colloids, 25(1), 522-528 (2008-12-09)
    The relative importance of electrostatic and nonelectrostatic interactions in peptide-microgel systems was evaluated by micromanipulator-assisted light microscopy, confocal microscopy, and circular dichroism. For this purpose, the interaction of various homopolypeptides with lightly cross-linked polyelectrolyte gel particles ( approximately 70 microm
    Noemi G Mirkin et al.
    Biopolymers, 97(10), 789-794 (2012-07-19)
    Although subsequent studies have provided extensive support for the 1968 Tiffany and Krimm proposal (Biopolymers 6, 1379) that the polyproline II (PPII) conformation is a significant component of the structure of unordered polypeptide chains, two issues are still not fully
    Stefania Conti et al.
    Biochimica et biophysica acta, 1828(3), 1066-1074 (2013-01-01)
    A proline-rich peptide of 2733Da, isolated from pig parotid granule preparations was tested against different pathogenic fungi. It showed interesting antifungal activity towards a clinical isolate of Cryptococcus neoformans, with an EC(50) of 2.2μM. Neither cytotoxic nor haemolytic effects were
    W Austin Elam et al.
    Protein science : a publication of the Protein Society, 22(4), 405-417 (2013-01-24)
    Intrinsically disordered (ID) proteins function in the absence of a unique stable structure and appear to challenge the classic structure-function paradigm. The extent to which ID proteins take advantage of subtle conformational biases to perform functions, and whether signals for
    M Rubert et al.
    Biomedical materials (Bristol, England), 7(5), 055003-055003 (2012-07-12)
    Polyproline-rich synthetic peptides have previously been shown to induce bone formation and mineralization in vitro and to decrease bone resorption in vivo. Alginate hydrogel formulations containing these synthetic peptides (P2, P5, P6) or Emdogain® (EMD) were tested for surface coating of

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