ZNF619 抗体 (AA 188-300) (AbBy Fluor® 594)
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北京 101111
Quick Overview for ZNF619 抗体 (AA 188-300) (AbBy Fluor® 594) (ABIN2807697)
抗原
See all ZNF619 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 188-300
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交叉反应
- 人
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纯化方法
- Purified by Protein A.
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免疫原
- KLH conjugated synthetic peptide derived from human ZNF619
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亚型
- IgG
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anti-Zinc Finger Protein 619 (ZNF619) (AA 72-121) antibody
ZNF619 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Zinc Finger Protein 619 (ZNF619) (AA 107-156) antibodyZNF619 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-Zinc Finger Protein 619 (ZNF619) (AA 114-143), (N-Term) antibodyZNF619 适用: 人 WB, FACS 宿主: 兔 Polyclonal RB28998 unconjugated
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应用备注
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IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200 -
限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 μg/μL
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缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
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储存液
- ProClin
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注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
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储存条件
- -20 °C
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储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
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有效期
- 12 months
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- ZNF619 (Zinc Finger Protein 619 (ZNF619))
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别名
- ZNF619
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背景
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Synonyms: FLJ90764, zinc finger protein 619, ZN619_HUMAN.
Background: Zinc-finger proteins contain DNA-binding domains and have a wide variety of functions, most of which encompass some form of transcriptional activation or repression. The majority of zinc-finger proteins contain a Kr_ppel-type DNA binding domain and a KRAB domain, which is thought to interact with KAP1, thereby recruiting histone modifying proteins. As a member of the krueppel C2H2-type zinc-finger protein family, ZNF619 (Zinc finger protein 619) is a 560 amino acid nuclear protein that contains ten C2H2-type zinc fingers. The gene encoding ZNF619 maps to human chromosome 3, which is made up of about 214 million bases encoding over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.
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基因ID
- 285267
抗原
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