电话:
400-7060-959
传真:
+86 10 56315212-8813
电子邮件:
orders@antibodies-online.cn

CFTR / Cystic Fibrosis Transmembrane Regulator 抗体

适用: 人, 小鼠 IHC (p) 宿主: 兔 Monoclonal CFTR-2290R unconjugated
产品编号 ABIN5707640
发货至: 中国
  • 抗原
    CFTR / Cystic Fibrosis Transmembrane Regulator
    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
    • 8
    • 4
    Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
    纯化方法
    Purified
    纯度
    Protein A affinity chromatography
    免疫原
    A recombinant human partial protein was used as the immunogen for this recombinant CFTR antibody.
    克隆位点
    CFTR-2290R
    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.\. Immunohistochemistry (FFPE): 0.5-1 μg/mL for 30 min at RT,Prediluted IHC only format: incubate for 30 min at RT (1)
    限制
    仅限研究用
  • 缓冲液
    0.2 mg/mL in 1X PBS with 0.1 mg/mL BSA (US sourced) and 0.05 % sodium azide
    储存液
    Sodium azide
    注意事项
    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
    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]
    基因ID
    1080
You are here:
客服