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PRNP 抗体

This anti-PRNP antibody is a 小鸡 多克隆 antibody detecting PRNP in WB, ICC 和 IF. Suitable for 人, 大鼠 和 小鼠.
产品编号 ABIN5540135
发货至: 中国

Quick Overview for PRNP 抗体 (ABIN5540135)

抗原

See all PRNP 抗体
PRNP (Prion Protein (PRNP))

适用

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人, 大鼠, 小鼠

宿主

  • 91
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  • 3
  • 2
小鸡

克隆类型

  • 81
  • 35
多克隆

标记

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This PRNP antibody is un-conjugated

应用范围

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Western Blotting (WB), Immunocytochemistry (ICC), Immunofluorescence (IF)
  • 纯化方法

    Purified

    免疫原

    Chickens were immunized with a recombinant fragment of the human prion protein emulsified with Freund's complete and incomplete adjuvants. After multiple injections, eggs were collected from the hens, and IgY fractions were prepared from the yolks. Affinity-purified antibodies were then prepared using an agarose column to which the recombinant protein fragments were covalently attached.Finally, affinity purified antibodies (50 ug/ml final concentration) were mixed with the IgY fraction (10 mg/ml final concentration) in a mixture containing glycerol (50% v/v) (to prevent freezing at -20°C) and 0.02% Sodium Azide.

    亚型

    Ig Fraction
  • 应用备注

    Western Blot: 1/2500. Immunohistochemistry: 1/1000-1/5000. Quality Control: Antibodies were analyzed by Immunocytochemistry (1/1000 dilution) using cells transfected with the prion protein cDNA.

    限制

    仅限研究用
  • 缓冲液

    Buffer System: 0.9 % (w/v) Sodium Phosphate (10 mM, pH 7.2) buffered isotonic saline, 50 % (v/v) Glycerol, with 0.02 % (w/v) Sodium Azide as an anti-microbial agent

    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

    -20 °C

    储存方法

    Upon receipt, store undiluted (in aliquots) at -20°C. This products is photosensitive and should be protected from light. Avoid repeated freezing and thawing. Shelf life: One year from despatch.
  • 抗原

    PRNP (Prion Protein (PRNP))

    别名

    cd230,prp

    背景

    Prion protein is the protein responsible for human Creutzfeldt-Jakob Disease (CJD), and somatic mutations of the prion gene are responsible for Gerstmann-Straussler-Scheinker disease and Fatal Familial Insomnia. The bovine homolog of the prion protein is responsible for bovine Spongioform Encephalopathy (BSE), also known as Mad Cow Disease. In all cases, the prion protein has two folding states, with one state being the normal non-pathological form, and the other state inducing a spongioform encephalopathy.

    UniProt

    P23907

    途径

    Transition Metal Ion Homeostasis, Activated T Cell Proliferation
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