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Merck
CN

A8052

Arg-Gly-Asp

≥97% (TLC)

别名:

L-arginyl-glycyl-L-aspartic acid

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关于此项目

经验公式(希尔记法):
C12H22N6O6
化学文摘社编号:
分子量:
346.34
NACRES:
NA.32
PubChem Substance ID:
UNSPSC Code:
12352209
MDL number:
Form:
powder
Assay:
≥97% (TLC)
Biological source:
synthetic
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biological source

synthetic

Quality Level

assay

≥97% (TLC)

form

powder

technique(s)

cell culture | stem cell: suitable

UniProt accession no.

storage temp.

−20°C

SMILES string

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

InChI

1S/C12H22N6O6/c13-6(2-1-3-16-12(14)15)10(22)17-5-8(19)18-7(11(23)24)4-9(20)21/h6-7H,1-5,13H2,(H,17,22)(H,18,19)(H,20,21)(H,23,24)(H4,14,15,16)/t6-,7-/m0/s1

InChI key

IYMAXBFPHPZYIK-BQBZGAKWSA-N

Gene Information

human ... FN1(2335)

General description

Arg-Gly-Asp(RGD)是整合素结合位点,属于粘附蛋白类。它可作为脑肿瘤靶向配体。

Application

Arg-Gly-Asp用于:
  • 使细胞表面Arg-Gly-Asp(RGD)受体饱和,抑制骨髓基质细胞(MSC)与肽修饰水凝胶的粘附
  • 粘附检测
  • 抑制实验,以证实细胞粘附的β1-整合素依赖性
  • 纺织品制造和RGD纺织品功能化
  • 构建迁移受损的人真皮成纤维细胞群
  • 修饰玻璃衬底并评估人骨髓间充质干细胞(hBM-MSC)的行为
  • 人乳腺上皮细胞的细胞培养

Biochem/physiol Actions

一级序列涉及蛋白与细胞表面的结合

Packaging

无底玻璃瓶。内容物在嵌入的融合锥中。

Preparation Note

来自纤连蛋白的细胞粘附结构域的三肽


存储类别

11 - Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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J Takagi
Biochemical Society transactions, 32(Pt3), 403-406 (2004-05-26)
Since the discovery of the RGD sequence motif as the essential cell attachment site in Fn (fibronectin), RGD-dependent ligand recognition by integrins has been the major focus of many integrin researches. Although many integrins recognize RGD-containing ligands, it is believed
Functional role of Arg-Gly-Asp (RGD)-binding sites on beta1 integrin in embryo implantation using mouse blastocysts and human decidua
Shiokawa S, et al.
Biology of Reproduction, 60(6), 1468-1474 (1999)
Leo J Hofland et al.
Journal of nuclear medicine : official publication, Society of Nuclear Medicine, 46 Suppl 1, 191S-198S (2005-01-18)
The presence of a high density of somatostatin receptors (SSRs) on human tumors forms the basis for the successful visualization of primary tumors and their metastases using radiolabeled somatostatin analogs. In recent years somatostatin analogs, coupled to beta-emitting radioisotopes, have



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