• merck millipore,默克密理博,MAB13489,Anti-MMP-2 Antibody, clone 1E4.2
  • merck millipore,默克密理博,MAB13489,Anti-MMP-2 Antibody, clone 1E4.2

    产品名称:Anti-MMP-2 Antibody, clone 1E4.2
    产品型号:MAB13489
    Anti-MMP-2 Antibody, clone 1E4.2 detects level of MMP-2 & has been published & validated for use in ELISA & WB.

    merck millipore,默克密理博,MAB13489,Anti-MMP-2 Antibody, clone 1E4.2

  • 产品介绍
  • merck millipore,默克密理博,MAB13489,Anti-MMP-2 Antibody, clone 1E4.2

    重要规格表

    品种反应性 主要应用 宿主 格式 抗体类型
    HWB, ELISAMPurifiedMonoclonal Antibody
    描述
    产品目录编号 MAB13489
    品牌系列 Chemicon®
    商名
    • Chemicon
    描述 Anti-MMP-2 Antibody, clone 1E4.2
    Alternate Names
    • 72 kDa Type IV Collagenase
    • Gelatinase A
    产品信息
    格式 Purified
    演示 Purified immunoglobulin. Liquid in PBS containing 0.01% sodium azide.
    应用
    应用 Anti-MMP-2 Antibody, clone 1E4.2 detects level of MMP-2 & has been published & validated for use in ELISA & WB.
    主要应用
    • Western Blotting
    • ELISA
    应用说明 Western blot: 1:200- 1:1000 Immunocytochemistry: Not Tested ELISA: 1:200-1:1000 Immunohistochemistry: Not Tested Optimal working dilutions must be determined by end user.
    生物信息
    免疫原品种 Purified Human MMP-2 (Gelatinase A)
    克隆 1E4.2
    浓缩 Please refer to the Certificate of Analysis for the lot-specific concentration.
    宿主 Mouse
    特异性 Human MMP-2 pro and active forms.
    同种型 IgG1
    品种反应性 Human
    抗体类型 Monoclonal Antibody
    Entrez基因编号
    • NM_004530.2
    Entrez基因汇总 Proteins of the matrix metalloproteinase (MMP) family are involved in the breakdown of extracellular matrix in normal physiological processes, such as embryonic development, reproduction, and tissue remodeling, as well as in disease processes, such as arthritis and metastasis. Most MMP's are secreted as inactive proproteins which are activated when cleaved by extracellular proteinases. This gene encodes an enzyme which degrades type IV collagen, the major structural component of basement membranes. The enzyme plays a role in endometrial menstrual breakdown, regulation of vascularization and the inflammatory response. Mutations in this gene have been associated with Winchester syndrome and Nodulosis-Arthropathy-Osteolysis (NAO) syndrome.
    基因符号
    • EC 3.4.24.24
    • MMP2
    • TBE-1
    • CLG4A
    • CLG4
    • MMP-II
    • MONA
    • MMP-2
    UniProt编号
    • P08253
    UniProt汇总 FUNCTION: SwissProt: P08253 # In addition to gelatin and collagens, it cleaves KiSS1 at a Gly- -Leu bond.
    COFACTOR: Binds 4 calcium ions per subunit. & Binds 2 zinc ions per subunit.
    SIZE: 660 amino acids; 73882 Da
    SUBUNIT: Ligand for integrin alpha-V/beta-3.
    TISSUE SPECIFICITY: Produced by normal skin fibroblasts.
    DOMAIN: SwissProt: P08253 The conserved cysteine present in the cysteine-switch motif binds the catalytic zinc ion, thus inhibiting the enzyme. The dissociation of the cysteine from the zinc ion upon the activation-peptide release activates the enzyme.
    PTM: The propeptide is processed by MMP14 (MT-MMP1) and MMP16 (MT- MMP3).
    DISEASE: SwissProt: P08253 # Defects in MMP2 are the cause of multicentric osteolysis nodulosis and arthropathy (MONA) [MIM:605156]. Inherited osteolyses or 'vanishing bone' syndromes are rare disorders of unknown etiology characterized by destruction and resorption of affected bones. MONA is an autosomal recessive osteolysis with multicentric involvement characterized by carpal and tarsal resorption, crippling arthritic changes, marked osteoporosis, palmar and plantar subcutaneous nodules and distinctive facies. & Defects in MMP2 are the cause of Winchester syndrome [MIM:277950]. Winchester syndrome is an autosomal recessive osteolysis syndrome. Winchester syndrome is severe with generalized osteolysis and osteopenia. Subcutaneous nodules are usually absent. Winchester syndrome has been associated with a number of additional features including coarse face, corneal opacities, patches of thickened, hyperpigmented skin, hypertrichosis and gum hypertrophy. However, these features are not always present and have occasionally been observed in other osteolysis syndromes. The clinical and molecular findings suggest that Winchester syndrome and MONA are allelic disorders that form a continuous clinical spectrum.
    SIMILARITY: Belongs to the peptidase M10A family. & Contains 3 fibronectin type-II domains. & Contains 4 hemopexin-like domains.
    产品使用声明
    使用声明
    • Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
    储存和货运信息
    存储条件 Maintain refrigerated at 2-8°C in undiluted aliquots for up to 6/12 months.
    包装信息
    数量 100 µg

    merck millipore,默克密理博,MAB13489,Anti-MMP-2 Antibody, clone 1E4.2

上一件merck millipore产品:merck millipore,默克密理博,14-596,LKB1/STRADα/MO25α Protein, active, 10 µg
下一件merck millipore产品:merck millipore,默克密理博,04-348,Anti-HER4/ErbB4 Antibody, clone E200, rabbit monoclonal



whatman,沃特曼,nalgene,耐洁,merck millipore,默克密理愽,sartorius,赛多利斯,pall,颇尔
thermo fisher,赛默飞世尔,GE,MN,macherey-nagel,advantec,wheaton,brand,普兰德,welch,airtech


上海羽令过滤器材有限公司版权所有 Copyright ©  www.yl-guolv.com  Powered by 羽令集团—信息技术部