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P3886

Poly-L-proline

Name: Poly-<SC>L</SC>-proline
Brand: SIGMA

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

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Informacje o tej pozycji

Wzór empiryczny (zapis Hilla):

C₅H₉NO₂

Numer CAS:

25191-13-3

Masa cząsteczkowa:

115.13

UNSPSC Code:

12352209

PubChem Substance ID:

24898465

NACRES:

NA.26

MDL number:

MFCD00166364

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Nazwa produktu

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

form

powder

Quality Level

200

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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Powiązane kategorie

Amino Acids – Building Blocks of Life Science

Biochemicals

Cell Culture Supplements & Reagents

Chemistry & Biochemicals

Analysis Note

Molecular weight based on viscosity.

Other Notes

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

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Klasa składowania

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Lot/Batch Number

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Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Interactions between homopolypeptides and lightly cross-linked microgels.

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

Water interaction differences determine the relative energetic stability of the polyproline II conformation of the alanine dipeptide in aqueous environments.

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

Evolutionary conservation of the polyproline II conformation surrounding intrinsically disordered phosphorylation sites.

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

Effect of alginate hydrogel containing polyproline-rich peptides on osteoblast differentiation.

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

Solvent interactions stabilize the polyproline II conformation of glycosylated oligoprolines.

Emmanuel B Naziga et al.

The journal of physical chemistry. B, 117(9), 2671-2681 (2013-02-01)

In nature, proline residues carry several post-translational modifications (PTMs), including 4R hydroxylation and glycosylation. A recent study synthesized contiguously hydroxylated and glycosylated nonaproline peptides and revealed that both PTMs lead to a significant increase in the thermal stability of PPII

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Produkty

Poly(Amino Acid) Block Copolymers for Drug Delivery and other Biomedical Applications

Humankind has utilized protein materials throughout its existence, starting with the use of materials such as wool and silk for warmth and protection from the elements and continuing with the use of recombinant DNA techniques to synthesize proteins with unique and useful properties.

Numer pozycji handlu globalnego

SKU	NUMER GTIN
P3886-500MG	04061832779683
P3886-1G	04061826659373

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