Citrullinated Histone H3 (human, recombinant)

Citrullinated Histone H3 (human, recombinant) (订货以CAS编码或英文名称为准)

Application|ELISA||Application|Western Blot||Product Type|Proteins||Research Area|Epigenetics, Transcription, & Translation|Histones/Histone Peptides|Citrullinated||Research Area|Epigenetics, Transcription, & Translation|Writers|Citrullination||Research Area|Immunology & Inflammation|Autoimmunity|Rheumatoid Arthritis||Research Area|Immunology & Inflammation|Innate Immunity|NETosis||Research Area|Immunology & Inflammation|Innate Immunity|Sepsis/Shock||Research Area|Neuroscience|Neurodegenerative Disorders|Multiple Sclerosis
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编号:PC55325
分子式:C19H18N2O4S
CAS号:477594-28-8
分子量:370.42
储存条件:-80
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货号 品牌 规格 纯度/含量 标准价 优惠价 库存货期 数量 购买
PC55325-10mg Medlife 10mg
≥95%
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PC55325-25mg Medlife 25mg
≥95%
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PC55325-50mg Medlife 50mg
≥95%
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PC55325-100mg Medlife 100mg
≥95%
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PC55325-100µg Medlife EA
¥7471.00 登录后可见
中文名称: 帕瑞昔布钠杂质34
中文别名: 帕瑞昔布钠杂质42;帕瑞昔布钠杂质46;帕瑞昔布杂质P:帕瑞昔布NO互换;匹杉琼杂质46;帕瑞昔布杂质006;帕雷昔布钠杂质34;帕瑞考昔钠杂质34;帕瑞昔布杂质38
英文名称: Citrullinated Histone H3 (human, recombinant)
英文别名: PROPANAMIDE, N-[[4-(3-METHYL-5-PHENYL-4-ISOXAZOLYL)PHENYL]SULFONYL]-;N-((4-(3-methyl-5-phenylisoxazol-4-yl)phenyl)sulfonyl)propionamide;Parecoxib Impurity P: Parecoxib NO Exchange;Parecoxib Impurity 46;Parecoxib Sodium-31;Parecoxib Sodium Impurity 46;Parecoxib Sodium Impurity 42;Parecoxib impurity 36/N-((4-(3-methyl-5-phenylisoxazol-4-yl)phenyl)sulfonyl)propionamide;Propanamide, N-[[4-(3-methyl-5-phenyl-4-isoxazolyl)phenyl]sulfonyl]-
CAS号: 477594-28-8
分子式: C19H18N2O4S
分子量: 370.42
详细描述 Application|ELISA||Application|Western Blot||Product Type|Proteins||Research Area|Epigenetics, Transcription, & Translation|Histones/Histone Peptides|Citrullinated||Research Area|Epigenetics, Transcription, & Translation|Writers|Citrullination||Research Area|Immunology & Inflammation|Autoimmunity|Rheumatoid Arthritis||Research Area|Immunology & Inflammation|Innate Immunity|NETosis||Research Area|Immunology & Inflammation|Innate Immunity|Sepsis/Shock||Research Area|Neuroscience|Neurodegenerative Disorders|Multiple Sclerosis
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