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Merck

A9041

Arg-Gly-Asp-Ser

≥95% (HPLC)

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Informazioni su questo articolo

Formula empirica (notazione di Hill):
C15H27N7O8
Numero CAS:
Peso molecolare:
433.42
NACRES:
NA.32
PubChem Substance ID:
UNSPSC Code:
12352209
MDL number:

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Nome del prodotto

Arg-Gly-Asp-Ser, ≥95% (HPLC)

InChI

1S/C15H27N7O8/c16-7(2-1-3-19-15(17)18)12(27)20-5-10(24)21-8(4-11(25)26)13(28)22-9(6-23)14(29)30/h7-9,23H,1-6,16H2,(H,20,27)(H,21,24)(H,22,28)(H,25,26)(H,29,30)(H4,17,18,19)/t7-,8-,9-/m0/s1

SMILES string

N[C@@H](CCCNC(N)=N)C(=O)NCC(=O)N[C@@H](CC(O)=O)C(=O)N[C@@H](CO)C(O)=O

InChI key

NNRFRJQMBSBXGO-CIUDSAMLSA-N

biological source

synthetic

assay

≥95% (HPLC)

form

powder

composition

Peptide content, ~70%

technique(s)

cell culture | mammalian: suitable

storage temp.

−20°C

Quality Level

Gene Information

human ... ITGA2B(3674), ITGB3(3690)
mouse ... Itgb3(16416)

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Questo articolo
G4391A8052SCP0156
Arg-Gly-Asp-Ser ≥95% (HPLC)

Sigma-Aldrich

A9041

Arg-Gly-Asp-Ser

Arg-Gly-Asp ≥97% (TLC)

Sigma-Aldrich

A8052

Arg-Gly-Asp

assay

≥95% (HPLC)

assay

≥97% (HPLC)

assay

≥97% (TLC)

assay

≥95% (HPLC)

biological source

synthetic

biological source

-

biological source

synthetic

biological source

-

technique(s)

cell culture | mammalian: suitable

technique(s)

blocking: suitable, cell culture | mammalian: suitable

technique(s)

cell culture | stem cell: suitable

technique(s)

-

form

powder

form

powder

form

powder

form

lyophilized

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

Gene Information

human ... ITGA2B(3674), ITGB3(3690)
mouse ... Itgb3(16416)

Gene Information

human ... ITGB3(3690)

Gene Information

human ... FN1(2335)

Gene Information

-

Application

Arg-Gly-Asp-Ser has been used:
  • to study its effects on cell attachment in rats[1]
  • to analyse the interaction of fibrinogen with erythrocytes occurs through integrin related receptor[2]
  • to pretreat the cells, to assess the role of integrin in the cell attachment process[3]
  • to test its competition with platelet-secreted, nanosheet-adsorbed proteins for binding to glycoprotein IIIa (GPIIIa)[4]

General description

The tetrapeptide Arg-Gly-Asp-Ser (RGDS) is a key component of the cell attachment domain of fibronectin. The RGDS sequence was found initially to promote the attachment of rat kidney fibroblasts (NRKcells) to fibronectin and synthetic fibronectin peptides coupled to protein-coated plastic. Further investigation indicated that the free RGDS peptide inhibited the attachment of NRK cells to fibronectin coated substrates. The RGDS sequence has been shown to occur in several other proteins, such as the λ receptor on E. coli and the Sindbis coat protein. RGDS is also a target sequence for spirochete adherence of the syphilis bacterium Treponema pallidum.

RGDS has been shown to block fibrinogen-induced aggregation of intact erythrocytes and specific binding of fibrinogen to erythrocyte membranes. The effect of RGDS on transforming growth factor ß1 (TGFß1) mRNA expression and secretion in cultured human mesangial cells has been investigated. RGDS has been utilized in a study of integrin-mediated signal transduction in cultured cells from the sponge Suberites domuncula. RGDS has been demonstrated
to mitigate the binding of Mycobacterium tuberculosis to murine alveolar macrophages

Other Notes

Lyophilized from 0.1% TFA in H2O

Packaging

Bottomless glass bottle. Contents are inside inserted fused cone.

Preparation Note

This product is soluble in water (1 mg/ml), yielding a
clear, colorless solution.

Classe di stoccaggio

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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Integrin and extracellular matrix interactions regulate engraftment of transplanted hepatocytes in the rat liver
Kumaran V, et al.
Gastroenterology, 129(5), 1643-1653 (2005)
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Molecular bioSystems, 8(4), 1264-1274 (2012-02-02)
We obtained novel peptides that selectively bind to self-assembling peptide nanomaterials from a random peptide library displayed on phages. Affinity-dependent peptide screening gave phage clones displaying peptides with selective affinities against two kinds of highly networked nanofibers constructed of β-sheet
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Proliferation and differentiation of cells are known to be influenced by the physical properties of the extracellular environment. Previous studies examining biophysics underlying cell response to matrix stiffness utilized a two-dimensional (2D) culture format, which is not representative of the
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