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首页  >  重组蛋白  >  Human EDN1 Recombinant Protein
EDN1 (基因名), Endothelin-1 (蛋白名), edn1_human.
产品名称:

Human EDN1/ Endothelin-1 Recombinant Protein
内皮素-1

货号:

R0482h

商标:
EIAab®
监管等级:
别名:

Preproendothelin-1, PPET1

序列号:
P05305
来源:
E.coli
种属:
Human
标签:
His
序列:
18aa-212aa
预估分子量:
21.45 kDa (monomer)
纯度:
Greater than 98% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
Cancer
  • Human EDN1 Protein
  • Human EDN1 Protein
  • Human EDN1 Protein
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Human EDN1 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
在线询价


R&D 技术数据
Human EDN1 Protein
The PCR product of human EDN1 gene was determined by 1% Agarose stained with EB.
Human EDN1 Protein
Recombinant human EDN1 protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: 6p24.1 by HGNC 6p24.1 by Entrez Gene 6p24.1 by Ensembl
EDN1 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
通用注释


亚单元:
N/A


功能:
Endothelins are endothelium-derived vasoconstrictor peptides.


亚细胞位置:
Secreted



[1].
"Investigating the association between K198N coding polymorphism in EDN1 and hypertension, lipoprotein levels, the metabolic syndrome and cardiovascular disease."

[2].
"Genetic analysis of 103 candidate genes for coronary artery disease and associated phenotypes in a founder population reveals a new association between endothelin-1 and high-density lipoprotein cholesterol."

[3].
"Evaluation of the Lys198Asn and -134delA genetic polymorphisms of the endothelin-1 gene."

[4].
"Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears."

[5].
"Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study."

[6].
"Investigating the association between K198N coding polymorphism in EDN1 and hypertension, lipoprotein levels, the metabolic syndrome and cardiovascular disease."

[7].
"Genetic analysis of 103 candidate genes for coronary artery disease and associated phenotypes in a founder population reveals a new association between endothelin-1 and high-density lipoprotein cholesterol."

[8].
"Evaluation of the Lys198Asn and -134delA genetic polymorphisms of the endothelin-1 gene."

[9].
"Mutations in endothelin 1 cause recessive auriculocondylar syndrome and dominant isolated question-mark ears."

[10].
"Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study."
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