• merck millipore,默克密理博,AB2043,Anti-Elastin Antibody
  • merck millipore,默克密理博,AB2043,Anti-Elastin Antibody

    产品名称:Anti-Elastin Antibody
    产品型号:AB2043
    Detect Elastin using this Anti-Elastin Antibody validated for use in ELISA, RIA, IH.

    merck millipore,默克密理博,AB2043,Anti-Elastin Antibody

  • 产品介绍
  • merck millipore,默克密理博,AB2043,Anti-Elastin Antibody

    重要规格表

    品种反应性 主要应用 宿主 格式 抗体类型
    HIHC, ELISARbPurifiedPolyclonal Antibody
    描述
    产品目录编号 AB2043
    品牌系列 Chemicon®
    商名
    • Chemicon
    描述 Anti-Elastin Antibody
    产品信息
    格式 Purified
    控制
    • Control tissue: human skin or liver
    演示 IgG fraction. Liquid in 0.01M Phosphate, 0.09M Sodium Chloride, pH 7.2, containing no preservatives.
    应用
    应用 Detect Elastin using this Anti-Elastin Antibody validated for use in ELISA, RIA, IH.
    主要应用
    • Immunohistochemistry
    • ELISA
    应用说明 Immunohistochemistry: 1:80 dilution for immunofluorescent staining of frozen human skin and liver tissues.

    Radioimmunoassay

    ELISA

    Optimal working dilutions must be determined by end user.
    生物信息
    免疫原品种 Elastin extracted and purified from human skin.
    浓缩 Please refer to the Certificate of Analysis for the lot-specific concentration.
    宿主 Rabbit
    特异性 Antibody shows less than 0.1% reactivity with human Collagen I, II, III, IV, V and human Fibronectin as well as Rat Elastin by radioimmunoassay.
    品种反应性 Human
    抗体类型 Polyclonal Antibody
    Entrez基因编号
    • NM_001081755.1
    • NM_000501.2
    • NM_001081752.1
    • NM_001081753.1
    • NM_001081754.1
    Entrez基因汇总 This gene encodes a protein that is one of the two components of elastic fibers. The encoded protein is rich in hydrophobic amino acids such as glycine and proline, which form mobile hydrophobic regions bounded by crosslinks between lysine residues. Deletions and mutations in this gene are associated with supravalvular aortic stenosis (SVAS) and autosomal dominant cutis laxa. Multiple transcript variants encoding different isoforms have been found for this gene.
    基因符号
    • WBS
    • ELN
    • tropoelastin
    • FLJ38671
    • SVAS
    • WS
    • Tropoelastin
    • elastin
    • FLJ43523
    非反应性品种
    • Rat
    UniProt编号
    • P15502
    UniProt汇总 FUNCTION: SwissProt: P15502 # Major structural protein of tissues such as aorta and nuchal ligament, which must expand rapidly and recover completely. Molecular determinant of the late arterial morphogenesis, stabilizing arterial structure by regulating proliferation and organization of vascular smooth muscle (By similarity).
    SIZE: 786 amino acids; 68499 Da
    SUBUNIT: The polymeric elastin chains are cross-linked together into an extensible 3D network. Forms a ternary complex with BGN and MFAP2. Interacts with MFAP2 via divalent cations (calcium > magnesium > manganese) in a dose-dependent and saturating manner.
    SUBCELLULAR LOCATION: Secreted, extracellular space, extracellular matrix. Note=Extracellular matrix of elastic fibers.
    TISSUE SPECIFICITY: Expressed within the outer myometrial smooth muscle and throughout the arteriolar tree of uterus (at protein level). Also expressed in the large arteries, lung and skin.
    PTM: Elastin is formed through the cross-linking of its soluble precursor tropoelastin. Cross-linking is initiated through the action of lysyl oxidase on exposed lysines to form allysine. Subsequent spontaneous condensation reactions with other allysine or unmodified lysine residues result in various bi-, tri-, and tetrafunctional cross-links. The most abundant cross-links in mature elastin fibers are lysinonorleucine, allysine aldol, desmosine, and isodesmosine. & Hydroxylation on proline residues within the sequence motif, GXPG, is most likely 4-hydroxy as this fits the requirement for 4- hydroxylation in vertebrates (By similarity).
    DISEASE: SwissProt: P15502 # Defects in ELN are a cause of autosomal dominant cutis laxa [MIM:123700]. Cutis laxa is a rare connective tissue disorder characterized by loose, hyperextensible skin with decreased resilience and elasticity leading to a premature aged appearance. The skin changes are often accompanied by extracutaneous manifestations, including pulmonary emphysema, bladder diverticula, pulmonary artery stenosis and pyloric stenosis. & Haploinsufficiency of ELN may be the cause of certain cardiovascular and musculo-skeletal abnormalities observed in Williams-Beuren syndrome (WBS) [MIM:194050]. WBS is a rare developmental disorder and a contiguous gene deletion syndrome involving genes from chromosome band 7q11.23. & Defects in ELN are the cause of supravalvular aortic stenosis (SVAS) [MIM:185500]. SVAS is a congenital narrowing of the ascending aorta which can occur sporadically, as an autosomal dominant condition, or as one component of Williams-Beuren syndrome.
    SIMILARITY: SwissProt: P15502 ## Belongs to the elastin family.
    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 frozen at -20°C for up to 12 months from date of receipt. Avoid repeated freeze/thaw cycles.
    包装信息
    数量 100 µg

    merck millipore,默克密理博,AB2043,Anti-Elastin Antibody

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