MYBPC1 抗体 (AA 51-150)
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- 抗原 See all MYBPC1 抗体
- MYBPC1 (Myosin Binding Protein C, Slow Type (MYBPC1))
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抗原表位
- AA 51-150
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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 MYBPC1 antibody is un-conjugated
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应用范围
- Western Blotting (WB), ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat,Dog,Sheep,Chicken
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human MYBPC1
- 亚型
- IgG
- Top Product
- Discover our top product MYBPC1 Primary Antibody
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- 应用备注
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WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500 - 限制
- 仅限研究用
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- 状态
- Liquid
- 浓度
- 1 μg/μL
- 缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: 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
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- MYBPC1 (Myosin Binding Protein C, Slow Type (MYBPC1))
- 别名
- MYBPC1 (MYBPC1 产品)
- 别名
- MYBPC1 antibody, zgc:92073 antibody, LCCS4 antibody, MYBPCC antibody, MYBPCS antibody, 8030451F13Rik antibody, myosin binding protein C, slow type antibody, myosin binding protein C, slow-type antibody, MYBPC1 antibody, mybpc1 antibody, Mybpc1 antibody
- 背景
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Synonyms: skeletal muscle slow isoform, slow-type, C protein, skeletal muscle slow isoform, C-protein, MYBPC1, MYBPCC, MYBPCS, Myosin binding protein C, slow type, Myosin-binding protein C, MYPC1_HUMAN, skeletal muscle C protein, Slow MyBP C, Slow MyBP-C.
Background: MYBPC1 is a 1,141 amino acid protein that contains three fibronectin type-III domains and seven Ig-like C2-type domains. Existing as a member of the immunoglobulin superfamily, MYBPC1 functions as a thick filament-associated protein that localizes to striated muscle bands in vertebrae and is thought to modify the activity of select ATPases. Additionally, MYBPC1 may play a role in the modulation of muscle contraction and in the overall structural integrity of the cell. The gene encoding MYBPC1 maps to human chromosome 12, which encodes over 1,100 genes and comprises approximately 4.5 % of the human genome. Chromosome 12 is associated with a variety of diseases and afflictions, including hypochondrogenesis, achondrogenesis, Kniest dysplasia, Noonan syndrome and Trisomy 12p, which causes facial developmental defects and seizure disorders.
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