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重組人層粘蛋白α2蛋白

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產(chǎn)品編號bs-10883P
英文名稱Recombinant human Laminin Subunit Alpha-2 protein, His
中文名稱重組人層粘蛋白α2蛋白
別    名LAMA 2; LAMA2; LAMA2; LAMA2_HUMAN; Laminin alpha 2 (merosin congenital muscular dystrophy); Laminin alpha 2; Laminin alpha 2 chain; Laminin alpha 2 subunit; Laminin M; Laminin M chain; Laminin subunit alpha-2; Laminin-12 subunit alpha; Laminin-2 subunit alpha; Laminin-4 subunit alpha; LAMM; LAMM; Merosin heavy chain; Merosin heavy chain; Laminin-12 subunit alpha; Recombinant human Laminin Subunit Alpha-2 protein, His  Laminin A2
理論分子量23kDa
檢測分子量24 kDa
性    狀Lyophilized or Liquid
濃    度>0.5 mg/ml
物    種Human
序    列381-580/3122
純    度>95% as determined by SDS-PAGE
純化方法AC
內毒素Not analyzed
表達系統(tǒng)E.coli
活性Not tested
標簽His
緩 沖 液20 mM Tris-HCl (pH=8.0) with 150 mM NaCl
保存條件Stored at -70℃ or -20℃. Avoid repeated freeze/thaw cycles.
注意事項This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
產(chǎn)品介紹Laminin, an extracellular protein, is a major component of the basement membrane. It is thought to mediate the attachment, migration, and organization of cells into tissues during embryonic development by interacting with other extracellular matrix components. It is composed of three subunits, alpha, beta, and gamma, which are bound to each other by disulfide bonds into a cross-shaped molecule. This gene encodes the alpha 2 chain, which constitutes one of the subunits of laminin 2 (merosin) and laminin 4 (s-merosin). Mutations in this gene have been identified as the cause of congenital merosin-deficient muscular dystrophy. Two transcript variants encoding different proteins have been found for this gene.

SWISS:
P24043

Gene ID:
3908

產(chǎn)品圖片
The purity of the protein is greater than 90% as determined by reducing SDS-PAGE.
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