- ￥1700 - 4000
- GeneTex
- 美国
- GTX113333
- 2025年07月16日
- WB
- Rabbit
- Human, Rat
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- 详细信息
- 文献和实验
- 技术资料
- 免疫原：
Recombinant protein encompassing a sequence within the C-terminus region of human Ceruloplasmin. The exact sequence is proprietary.
- 亚型：
IgG
- 形态：
Liquid
- 保存条件：
Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
- 克隆性：
Polyclonal
- 标记物：
Unconjugated
- 适应物种：
Human, Rat
- 保质期：
12 months from the shipping date of the product.
- 抗原来源：
Human
- 目录编号：
GTX113333
- 级别：
Primary Antibodies
- 库存：
Available
- 供应商：
GeneTex
- 宿主：
Rabbit
- 应用范围：
WB
- 浓度：
0.65 mg/ml (Please refer to the vial label for the specific concentration.)
- 靶点：
Ceruloplasmin
- 抗体英文名：
Ceruloplasmin antibody
- 抗体名：
Ceruloplasmin 抗体
- 规格：
100 μl/25 μl
| 规格： | 100 μl | 产品价格： | ￥4000.0 |
|---|---|---|---|
| 规格： | 25 μl | 产品价格： | ￥1700.0 |
Ceruloplasmin antibody [C2C3], C-term detects Ceruloplasmin [C2C3], C-term protein by western blot analysis. Human tissue extracts (30 μg) was separated by 5% SDS-PAGE, and the membrane was blotted with Ceruloplasmin antibody [C2C3], C-term (GTX113333) diluted at 1:1000.
Rat tissue extract (50 μg) was separated by 5% SDS-PAGE, and the membrane was blotted with Ceruloplasmin antibody (GTX113333) diluted at 1:500.
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文献和实验铜蓝蛋白（ceruloplasmin,CER）是一种含铜的α2 糖蛋白，分子量约为12万-16万，不易纯化。目前所知为一个单链多肽，每分子含6-7个铜原子，由于含铜而呈蓝色，含糖约10%，末端唾液酸与多肽链连接，具有遗传上的基因多形性。 CER具有氧化酶的活性，对多酚及多胺类底物有催化其氧化的能力。最近研究认为CER可催化Fe2 氧化为Fe3 。对于CER是否是铜的载体存在不同看法。血清中铜的含量虽有95%以非扩散状态处于CER，而有5%呈可透析状态由肠管
Ceruloplasmin Detection by SDS-PAGE, Immunoblotting, and In Situ Oxidase Activity
Ceruloplasmin is an acute-phase reactant that functions as a ferroxidase, oxidizing Fe++ to Fe+++ , the latter being able to combine with apotransferrin to form transferrin, the primary iron transport protein in the plasma. Ferroxidases
Generation of Antibody Molecules Through Antibody Engineering
been overcome to a large extent using genetic-engineering techniques to produce chimeric mouse/human and completely human antibodies. Such an approach is particularly suitable because of the domain structure of the antibody molecule ( 2 ), where functional
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