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MYL3 (基因名), Myosin light chain 3 (蛋白名), myl3_human.
产品名称:

Human MYL3/ Myosin light chain 3 Recombinant Protein
肌球蛋白轻链3

货号:

R1391h

商标:
EIAab®
监管等级:
别名:

Cardiac myosin light chain 1, Myosin light chain 1, slow-twitch muscle B/ventricular isoform, Ventricular myosin alkali light chain, Ventricular myosin light chain 1, Ventricular/slow twitch myosin alkali light chain, CMLC1, MLC1SB, VLCl, MLC-lV/sb

序列号:
P08590
来源:
E.coli
种属:
Human
标签:
His
序列:
1-195aa
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:
Signal Transduction
  • Human MYL3 Protein
  • Human MYL3 Protein
  • Human MYL3 Protein
规格 & 价格: cart
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Human MYL3 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 MYL3 Protein
The PCR product of human MYL3 gene was determined by 1% Agarose stained with EB.
Human MYL3 Protein
Recombinant human MYL3 protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: 3p21.31 by HGNC 3p21.31 by Entrez Gene 3p21.31 by Ensembl
MYL3 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:
Myosin is a hexamer of 2 heavy chains and 4 light chains.


功能:
Regulatory light chain of myosin. Does not bind calcium.


亚细胞位置:
N/A


该产品尚未在任何出版物中被引用。

[1].
"The role of sarcomere gene mutations in patients with idiopathic dilated cardiomyopathy."

[2].
"Systematic analysis of the regulatory and essential myosin light chain genes: genetic variants and mutations in hypertrophic cardiomyopathy."

[3].
"Clinical features and outcome of hypertrophic cardiomyopathy associated with triple sarcomere protein gene mutations."

[4].
"Variation at the NFATC2 locus increases the risk of thiazolidinedione-induced edema in the Diabetes REduction Assessment with ramipril and rosiglitazone Medication (DREAM) study."

[5].
"Histologic characterization of hypertrophic cardiomyopathy with and without myofilament mutations."

[6].
"Prevalence of sarcomere protein gene mutations in preadolescent children with hypertrophic cardiomyopathy."

[7].
"Shared genetic causes of cardiac hypertrophy in children and adults."

[8].
"Relationship between sex, shape, and substrate in hypertrophic cardiomyopathy."

[9].
"Minigenes encoding N-terminal domains of human cardiac myosin light chain-1 improve heart function of transgenic rats."

[10].
"Single-gene mutations and increased left ventricular wall thickness in the community: the Framingham Heart Study."
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