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- 抗原 See all EVC2 抗体
- EVC2 (Ellis Van Creveld Syndrome 2 (EVC2))
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抗原表位
- C-Term
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This EVC2 antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunofluorescence (IF), Immunocytochemistry (ICC)
- 交叉反应
- 小鼠
- 交叉反应 （详细）
- Mouse (85 %)
- 产品特性
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Rabbit Polyclonal antibody to EVC2 (Ellis van Creveld syndrome 2)
EVC2 antibody [C3], C-term - 纯化方法
- Purified by antigen-affinity chromatography.
- 免疫原
- Carrier-protein conjugated synthetic peptide encompassing a sequence within the C-terminus region of human EVC2. The exact sequence is proprietary.
- 亚型
- IgG
- Top Product
- Discover our top product EVC2 Primary Antibody
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anti-Ellis Van Creveld Syndrome 2 (EVC2) (AA 30-199) antibody
EVC2 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Ellis Van Creveld Syndrome 2 (EVC2) antibodyEVC2 适用: 人, 小鼠 ELISA, IHC, WB 宿主: 兔 Polyclonal unconjugated
anti-Ellis Van Creveld Syndrome 2 (EVC2) (C-Term) antibodyVerified EVC2 适用: 人 ELISA, IHC 宿主: 山羊 Polyclonal unconjugated
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- 应用备注
- Suggested dilution Reference ICC/IF 1:100-1:1000* Western blot 1:500-1:3000* Not tested in other applications. *Optimal dilutions/concentrations should be determined by the researcher.Suggested dilutionReferenceICC/IF1:100-1:1000* Western blot1:500-1:3000*
- 说明
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Positive Control: A431 , H1299 , HeLa , HepG2
- 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 mg/mL
- 缓冲液
- 0.1M Tris, 0.1M Glycine, 10 % Glycerol ( pH 7). 0.01 % Thimerosal was added as a preservative.
- 储存液
- Thimerosal (Merthiolate)
- 注意事项
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Keep as concentrated solution. Aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- 抗原
- EVC2 (Ellis Van Creveld Syndrome 2 (EVC2))
- 别名
- EVC2 (EVC2 产品)
- 别名
- EVC2 antibody, LBN antibody, 1110017L09Rik antibody, Lbn antibody, limbin antibody, EvC ciliary complex subunit 2 antibody, EVC2 antibody, Evc2 antibody
- 背景
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This gene encodes a protein that functions in bone formation and skeletal development. Mutations in this gene, as well as in a neighboring gene that lies in a head-to-head configuration, cause Ellis-van Creveld syndrome, an autosomal recessive skeletal dysplasia that is also known as chondroectodermal dysplasia. Mutations in this gene also cause acrofacial dysostosis Weyers type, also referred to as Curry-Hall syndrome, a disease that combines limb and facial abnormalities. Alternative splicing results in multiple transcript variants.
Cellular Localization: Membrane, Multi-pass membrane protein - 分子量
- 148 kDa
- 基因ID
- 132884
- 途径
- Hedgehog Signaling
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