CCDC38 抗体 (AA 451-563) (Cy5)
Quick Overview for CCDC38 抗体 (AA 451-563) (Cy5) (ABIN887683)
抗原
See all CCDC38 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 451-563
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预测反应
- Human,Mouse,Rat,Dog,Cow,Pig,Horse,Chicken,Rabbit
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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 CCDC38
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亚型
- IgG
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anti-Coiled-Coil Domain Containing 38 (CCDC38) (AA 143-192) antibody
CCDC38 适用: 人, 小鼠, 大鼠, Cow, 犬, 马, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Coiled-Coil Domain Containing 38 (CCDC38) (N-Term) antibodyCCDC38 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Coiled-Coil Domain Containing 38 (CCDC38) (AA 352-380) antibodyCCDC38 适用: 人, 小鼠 WB, IHC (p) 宿主: 兔 Polyclonal RB28590 unconjugated
anti-Coiled-Coil Domain Containing 38 (CCDC38) (N-Term) antibodyCCDC38 适用: 人, 小鼠, 大鼠, Cow, 犬, 马, 豚鼠, Pig, 兔 WB 宿主: 兔 Polyclonal unconjugated
anti-Coiled-Coil Domain Containing 38 (CCDC38) (AA 359-388), (Middle Region) antibodyCCDC38 适用: 人, 小鼠 WB, IHC (p), EIA 宿主: 兔 Polyclonal 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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- CCDC38 (Coiled-Coil Domain Containing 38 (CCDC38))
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别名
- CCDC38
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背景
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Synonyms: CCDC38 coiled coil domain containing 38, Coiled coil domain containing 38, FLJ40089, CCD38_HUMAN.
Background: The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion and drug extrusion and delivery. CCDC38 (coiled-coil domain containing 38) is a 563 amino acid protein encoded by a gene that maps to human chromosome 12q23.1. Encoding over 1,100 genes, chromosome 12 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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基因ID
- 120935
抗原
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