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Fibrillin 1 抗体

This 兔 多克隆 antibody specifically detects Fibrillin 1 in WB 和 ELISA. It exhibits reactivity toward 人 和 犬.
产品编号 ABIN2461618
发货至: 中国
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Quick Overview for Fibrillin 1 抗体 (ABIN2461618)

抗原

See all Fibrillin 1 (FBN1) 抗体
Fibrillin 1 (FBN1)

适用

  • 68
  • 34
  • 25
  • 11
  • 3
  • 2
  • 2
  • 2
  • 1
  • 1
人, 犬

宿主

  • 79
  • 12
  • 1

克隆类型

  • 81
  • 11
多克隆

标记

  • 47
  • 15
  • 11
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This Fibrillin 1 antibody is un-conjugated

应用范围

  • 58
  • 33
  • 28
  • 17
  • 15
  • 13
  • 13
  • 12
  • 12
  • 11
  • 5
  • 3
  • 2
  • 1
Western Blotting (WB), ELISA
  • 纯化方法

    Antibody is purified by peptide affinity chromatography method.

    免疫原

    Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human FBN1.
  • 应用备注

    FBN1 antibody can be used for detection of FBN1 by ELISA at 1:1562500. FBN1 antibody can be used for detection of FBN1 by western blot at 0.25 μg/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.

    限制

    仅限研究用
  • 状态

    Lyophilized

    溶解方式

    Add 50 ?L of distilled water. Final antibody concentration is 1 mg/mL.

    浓度

    1 mg/mL

    缓冲液

    Antibody is lyophilized in PBS buffer with 2 % sucrose.

    注意事项

    As with any antibody avoid repeat freeze-thaw cycles.

    储存条件

    4 °C/-20 °C

    储存方法

    For short periods of storage (days) store at 4 °C. For longer periods of storage, store FBN1 antibody at -20 °C.
  • 抗原

    Fibrillin 1 (FBN1)

    别名

    FBN1

    背景

    FBN1 is a member of the fibrillin family. FBN1 is a large, extracellular matrix glycoprotein that serve as a structural component of 10-12 nm calcium-binding microfibrils. These microfibrils provide force bearing structural support in elastic and nonelastic connective tissue throughout the body. Mutations in this gene are associated with Marfan syndrome, isolated ectopia lentis, autosomal dominant Weill-Marchesani syndrome, MASS syndrome, and Shprintzen-Goldberg craniosynostosis syndrome.

    分子量

    21 kDa, 312 kDa

    基因ID

    2200

    UniProt

    Q75N89

    途径

    Maintenance of Protein Location, SARS-CoV-2 Protein Interactome
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