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LAMA2 (基因名), Laminin subunit alpha-2 (蛋白名), lama2_human.
产品名称:

Human LAMA2/ Laminin subunit alpha-2 Recombinant Protein
层粘连蛋白亚基α2

货号:

R9489h

商标:
EIAab®
监管等级:
别名:

Laminin M chain, Laminin-12 subunit alpha, Laminin-2 subunit alpha, Laminin-4 subunit alpha, Merosin heavy chain, LAMM

序列号:
P24043
来源:
E.coli
种属:
Human
标签:
His
纯度:
>90% 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:
-
Human LAMA2 Protein
规格 & 价格: cart
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Human LAMA2 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
更多信息,请参阅手册,或联系我们的技术支持: tech@eiaab.com.
基因位点
Cytogenetic band: 6q22.33 by HGNC 6q22.33 by Entrez Gene 6q22.33 by Ensembl
LAMA2 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:
Laminin is a complex glycoprotein, consisting of three different polypeptide chains (alpha, beta, gamma), which are bound to each other by disulfide bonds into a cross-shaped molecule comprising one long and three short arms with globules at each end. Alpha-2 is a subunit of laminin-2 (laminin-211 or merosin), laminin-4 (laminin-221 or S-merosin) and laminin-12 (laminin-213). Interacts with FBLN1, FBLN2 and NID2.


功能:
Binding to cells via a high affinity receptor, laminin is thought to mediate the attachment, migration and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components.


亚细胞位置:
Secreted Extracellular space Extracellular matrix Basement membrane Major component.


该产品尚未在任何出版物中被引用。

[1].
"Human laminin M chain (merosin): complete primary structure, chromosomal assignment, and expression of the M and A chain in human fetal tissues."

[2].
"Clinical and molecular study in congenital muscular dystrophy with partial laminin alpha 2 (LAMA2) deficiency."

[3].
"Congenital muscular dystrophy with primary partial laminin alpha2 chain deficiency: molecular study."

[4].
"Structure of the human laminin alpha2-chain gene (LAMA2), which is affected in congenital muscular dystrophy."

[5].
"Merosin, a tissue-specific basement membrane protein, is a laminin-like protein."
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