DLL3 抗体 (AA 400-618)
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Quick Overview for DLL3 抗体 (AA 400-618) (ABIN7874782)
抗原
See all DLL3 抗体适用
宿主
克隆类型
标记
应用范围
克隆位点
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抗原表位
- AA 400-618
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原理
- DLL3 Antibody / Delta-like protein 3
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纯化方法
- Protein A/G affinity
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免疫原
- A portion of amino acids 400-618 from human DLL3 protein was used as the immunogen for the DLL3 antibody.
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亚型
- IgG2c, kappa
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anti-delta Like Protein 3 (DLL3) (AA 545-573), (C-Term) antibody
DLL3 适用: 人 WB, IF, IHC (p) 宿主: 兔 Polyclonal RB31357 unconjugated
anti-delta Like Protein 3 (DLL3) (AA 519-548), (C-Term) antibodyDLL3 适用: 人, 小鼠, 大鼠 WB, IF, IHC (p) 宿主: 兔 Polyclonal RB23871 unconjugated
anti-delta Like Protein 3 (DLL3) (AA 519-548) antibodyDLL3 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-delta Like Protein 3 (DLL3) antibodyDLL3 适用: 小鼠, 大鼠 IHC 宿主: 兔 Polyclonal unconjugated
anti-delta Like Protein 3 (DLL3) (AA 27-492) antibodyDLL3 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-delta Like Protein 3 (DLL3) (AA 526-556), (C-Term) antibodyDLL3 适用: 人 WB, IF, IHC (p), EIA 宿主: 兔 Polyclonal unconjugated
anti-delta Like Protein 3 (DLL3) (AA 100-150) antibodyDLL3 适用: 人, 小鼠, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-delta Like Protein 3 (DLL3) antibodyDLL3 适用: 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-delta Like Protein 3 (DLL3) (AA 599-618), (C-Term) antibodyDLL3 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
anti-delta Like Protein 3 (DLL3) (AA 599-618) antibodyDLL3 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
- Optimal dilution of the DLL3 antibody should be determined by the researcher.
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 0.2 mg/mL
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缓冲液
- 0.2 mg/mL in 1X PBS with 0.1 mg/mL BSA (US sourced), 0.05 % sodium azide
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储存液
- Sodium azide
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注意事项
- This product contains Sodium azide: 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
- Aliquot the DLL3 antibody and store frozen at -20oC or colder. Avoid repeated freeze-thaw cycles.
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- DLL3 (delta Like Protein 3 (DLL3))
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别名
- DLL3
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背景
- This gene encodes a member of the delta protein ligand family. This family functions as Notch ligands that are characterized by a DSL domain, EGF repeats, and a transmembrane domain. Mutations in this gene cause autosomal recessive spondylocostal dysostosis 1. Two transcript variants encoding distinct isoforms have been identified for this gene.
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UniProt
- Q9NYJ7
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途径
- Notch Signaling
抗原
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