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Recombinant CFTR / Cystic Fibrosis Transmembrane Regulator 抗体

The 兔 单克隆 anti-CFTR / Cystic Fibrosis Transmembrane Regulator antibody (Clone CFTR-2290R) (ABIN5707642) specifically detects CFTR / Cystic Fibrosis Transmembrane Regulator in IHC (p). The antibody is reactive with 人 和 小鼠 samples.
产品编号 ABIN5707642
发货至: 中国
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Quick Overview for Recombinant CFTR / Cystic Fibrosis Transmembrane Regulator 抗体 (ABIN5707642)

抗原

CFTR / Cystic Fibrosis Transmembrane Regulator

抗体类型

Recombinant Antibody

适用

人, 小鼠

宿主

  • 6
  • 3

克隆类型

  • 9
单克隆

标记

  • 9
非结合性

应用范围

  • 9
  • 2
Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

质量等级

Carrier-free

克隆位点

CFTR-2290R
  • 原理

    Recombinant CFTR Antibody / Rabbit Monoclonal (azide and preservative free)

    纯化方法

    Protein A affinity chromatography

    免疫原

    A recombinant human partial protein was used as the immunogen for this recombinant CFTR antibody.

    亚型

    IgG, kappa
  • 应用备注

    Optimal dilution of the recombinant CFTR antibody should be determined by the researcher.

    1. The prediluted format is supplied in a dropper bottle and is optimized for use in IHC. After epitope retrieval step (if required), drip mAb solution onto the tissue section and incubate at RT for 30 min.

    限制

    仅限研究用
  • 状态

    Liquid

    浓度

    1 mg/mL

    缓冲液

    1 mg/mL in 1X PBS, BSA free, sodium azide free

    储存液

    Azide free

    储存条件

    4 °C,-20 °C

    储存方法

    Store the recombinant CFTR antibody at 2-8oC (with azide) or aliquot and store at -20oC or colder (without azide).
  • 抗原

    CFTR / Cystic Fibrosis Transmembrane Regulator

    背景

    Cystic fibrosis transmembrane conductance regulator (CFTR) is a membrane protein and chloride channel in vertebrates that is encoded by the CFTR gene. The CFTR gene codes for an ABC transporter-class ion channel protein that conducts chloride and thiocyanate ions across epithelial cell membranes. Mutations of the CFTR gene affecting chloride ion channel function lead to dysregulation of epithelial fluid transport in the lung, pancreas and other organs, resulting in cystic fibrosis. Complications include thickened mucus in the lungs with frequent respiratory infections, and pancreatic insufficiency giving rise to malnutrition and diabetes. These conditions lead to chronic disability and reduced life expectancy. In male patients, the progressive obstruction and destruction of the developing vas deferens (spermatic cord) and epididymis appear to result from abnormal intraluminal secretions, causing congenital absence of the vas deferens and male infertility. [Wiki]

    UniProt

    P13569
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