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MFAP3 抗体 (AA 19-349)

This 兔 多克隆 antibody specifically detects MFAP3 in ELISA, WB, FACS 和 IHC (p). It exhibits reactivity toward 人, 小鼠 和 大鼠.
产品编号 ABIN7871588
发货至: 中国
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Quick Overview for MFAP3 抗体 (AA 19-349) (ABIN7871588)

抗原

See all MFAP3 抗体
MFAP3 (Microfibrillar Associated Protein 3 (MFAP3))

适用

人, 小鼠, 大鼠

宿主

  • 8
  • 5

克隆类型

  • 9
  • 4
多克隆

标记

  • 9
  • 2
  • 1
  • 1
This MFAP3 antibody is un-conjugated

应用范围

  • 8
  • 6
  • 3
  • 2
  • 2
  • 2
  • 1
ELISA, Western Blotting (WB), Flow Cytometry (FACS), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
  • 抗原表位

    • 5
    • 1
    • 1
    • 1
    AA 19-349

    原理

    MFAP3 Antibody / Microfibril-associated glycoprotein 3

    纯化方法

    Antigen affinity purified

    免疫原

    An E.coli-derived human recombinant protein (A19-N349) was used as the immunogen for the MFAP3 antibody.

    亚型

    IgG
  • 应用备注

    Optimal dilution of the MFAP3 antibody should be determined by the researcher.

    限制

    仅限研究用
  • 状态

    Lyophilized

    缓冲液

    0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

    储存条件

    4 °C,-20 °C

    储存方法

    After reconstitution, the MFAP3 antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.
  • 抗原

    MFAP3 (Microfibrillar Associated Protein 3 (MFAP3))

    别名

    MFAP3

    背景

    Microfibril-associated glycoprotein 3 (MFAP3), is a member of the MFAP family which play a role in microfibril assembly, elastinogenesis, and tissue homeostasis. The family members were identified as potential components of fibrillin-containing microfibrils, but they do not share structural similarities. MFAP3 is found in ocular zonules. Human MFAP3 is a serine-rich acidic protein located in zonular fibers and consists of an extracellular domain (ECD) containing one Ig-like C2-type domain, a single transmembrane domain, and a cytoplasmic domain. Within the ECD, mature human MFAP3 shares 74 % amino acid sequence identity with mouse and rat MFAP3. Among MFAP3-related pathways are degradation of the extracellular matrix and elastic fiber formation. MFAP is a candidate gene for heritable diseases affecting microfibrils.

    UniProt

    P55082
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