• merck millipore,默克密理博,AB757P,Anti-Collagen Type III Antibody
  • merck millipore,默克密理博,AB757P,Anti-Collagen Type III Antibody

    产品名称:Anti-Collagen Type III Antibody
    产品型号:AB757P
    Detect Collagen Type III using this Anti-Collagen Type III Antibody validated for use in ELISA, RIA, IH.

    merck millipore,默克密理博,AB757P,Anti-Collagen Type III Antibody

  • 产品介绍
  • merck millipore,默克密理博,AB757P,Anti-Collagen Type III Antibody

    重要规格表

    品种反应性 主要应用 宿主 格式 抗体类型
    RIHC, ELISARbPurifiedPolyclonal Antibody
    描述
    产品目录编号 AB757P
    Replaces AB757
    品牌系列 Chemicon®
    商名
    • Chemicon
    描述 Anti-Collagen Type III Antibody
    概述 Collagen Type III extracted and purified from rat skin. Antibody shows less than 0.1% reactivity with rat Collagen Type I and rat Elastin with less than 10.0% reactivity with rat Collagen Type V.
    产品信息
    格式 Purified
    演示 Affinity purified immunoglobulin. Liquid, containing 0.01M phosphate, 0.09M NaCl, pH 7.2. No preservatives.
    应用
    应用 Detect Collagen Type III using this Anti-Collagen Type III Antibody validated for use in ELISA, RIA, IH.
    主要应用
    • Immunohistochemistry
    • ELISA
    不建议的应用
    • Western Blotting
    应用说明 Immunohistochemistry: 1:80 dilution for immunofluorescent staining of frozen rat skin and liver tissues.

    Radioimmunoassay

    ELISA: 1:1000

    Not recommended for paraffin tissue sections or Western blots.

    Optimal working dilutions must be determined by the end user.
    生物信息
    浓缩 Please refer to the Certificate of Analysis for the lot-specific concentration.
    宿主 Rabbit
    特异性 Rat Type III 100%

    Rat Type I < 0.1%

    Rat Type V 9%

    Mouse Type III 9%

    Human Type I < 0.1%

    Rat Elastin < 0.1%
    品种反应性 Rat
    抗体类型 Polyclonal Antibody
    Entrez基因编号
    • NM_000090.3
    Entrez基因汇总 This gene encodes the pro-alpha1 chains of type III collagen, a fibrillar collagen that is found in extensible connective tissues such as skin, lung, uterus, intestine and the vascular system, frequently in association with type I collagen. Mutations in this gene are associated with Ehlers-Danlos syndrome types IV, and with aortic and arterial aneurysms. Two transcripts, resulting from the use of alternate polyadenylation signals, have been identified for this gene. [provided by R. Dalgleish]
    基因符号
    • FLJ34534
    • COL3A1
    • EDS4A
    UniProt编号
    • P02461
    UniProt汇总 FUNCTION: SwissProt: P02461 # Collagen type III occurs in most soft connective tissues along with type I collagen.
    SIZE: 1466 amino acids; 138564 Da
    SUBUNIT: Trimers of identical alpha 1(III) chains. The chains are linked to each other by interchain disulfide bonds. Trimers are also cross-linked via hydroxylysines.
    SUBCELLULAR LOCATION: Secreted, extracellular space, extracellular matrix (By similarity).
    PTM: Proline residues at the third position of the tripeptide repeating unit (G-X-Y) are hydroxylated in some or all of the chains. & O-linked glycan consists of a Glc-Gal disaccharide bound to the oxygen atom of a post-translationally added hydroxyl group.
    DISEASE: SwissProt: P02461 # Defects in COL3A1 are a cause of Ehlers-Danlos syndrome type III (EDS-III) [MIM:130020]; also known as benign hypermobility syndrome. Inheritance is autosomal dominant. EDS is characterized by joint laxity and hyperextensible skin. It is divided into nine different subtypes based on biochemical and clinical variations. & Defects in COL3A1 are the cause of Ehlers-Danlos syndrome type IV (EDS-IV) [MIM:130050]. EDS-IV is the most severe form of the disease, in that it often produces life-threatening consequences, such as rupture of the arteries, bowel, or uterus. A variant form of EDS-IV is Gottron type acrogeria [MIM:201200]. The main characteristics are atrophy and mottled-type hyperpigmentation of the acral skin, resulting in an aged appearance. & Defects in COL3A1 may be a cause of aortic aneurysm [MIM:100070]. Aortic aneurysm consists of a dangerous ballooning of the aorta which is caused by a defect in the artery's wall.
    SIMILARITY: SwissProt: P02461 ## Belongs to the fibrillar collagen family. & Contains 1 VWFC domain.
    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 after date of receipt. Avoid repeated freeze/thaw cycles.
    包装信息
    数量 100 µg

    merck millipore,默克密理博,AB757P,Anti-Collagen Type III Antibody

上一件merck millipore产品:merck millipore,默克密理博,05-170,Anti-IL-2 Rα Antibody, clone 7G7/B6
下一件merck millipore产品:merck millipore,默克密理博,S7250,OxyELISA™ Oxidized Protein Quantitation Kit



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