CLN5 抗体 (AA 171-220)
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北京 101111
Quick Overview for CLN5 抗体 (AA 171-220) (ABIN1451151)
抗原
See all CLN5 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 171-220
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原理
- CLN5 Antibody
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特异性
- CLN5 Polyclonal Antibody detects endogenous levels of CLN5 protein.
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纯化方法
- The antibody was affinity-purified from rabbit antiserum by affinity-chromatography using epitope-specific immunogen.
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免疫原
- The antiserum was produced against synthesized peptide derived from human CLN5. AA range:171-220
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亚型
- IgG
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anti-Ceroid-Lipofuscinosis, Neuronal 5 (CLN5) (AA 42-181) antibody
CLN5 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-Ceroid-Lipofuscinosis, Neuronal 5 (CLN5) antibodyCLN5 适用: 人, 大鼠, 小鼠 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Ceroid-Lipofuscinosis, Neuronal 5 (CLN5) (AA 96-407) antibodyCLN5 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-Ceroid-Lipofuscinosis, Neuronal 5 (CLN5) (AA 41-69), (N-Term) antibodyCLN5 适用: 人 WB 宿主: 兔 Polyclonal RB23453 unconjugated
anti-Ceroid-Lipofuscinosis, Neuronal 5 (CLN5) (Internal Region) antibodyCLN5 适用: 人, 大鼠, 小鼠 WB, IF, ICC 宿主: 兔 Polyclonal unconjugated
anti-Ceroid-Lipofuscinosis, Neuronal 5 (CLN5) (Internal Region) antibodyCLN5 适用: 人, 大鼠, 小鼠 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Ceroid-Lipofuscinosis, Neuronal 5 (CLN5) (AA 1-407) antibodyCLN5 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
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应用备注
- WB 1:500 - 1:2000. ELISA: 1:10000. Not yet tested in other applications.
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限制
- 仅限研究用
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状态
- Liquid
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浓度
- 1 mg/mL
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缓冲液
- Liquid in PBS containing 50 % glycerol, 0.5 % BSA and 0.02 % 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
- Store at -20°C/1 year
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有效期
- 12 months
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- CLN5 (Ceroid-Lipofuscinosis, Neuronal 5 (CLN5))
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别名
- CLN5
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背景
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Synonyms: CLN5, Ceroid-lipofuscinosis neuronal protein 5, Protein CLN5
Background: ceroid-lipofuscinosis, neuronal 5(CLN5) Homo sapiens This gene is one of eight which have been associated with neuronal ceroid lipofuscinoses (NCL). Also referred to as Batten disease, NCL comprises a class of autosomal recessive, neurodegenerative disorders affecting children. The genes responsible likely encode proteins involved in the degradation of post-translationally modified proteins in lysosomes. The primary defect in NCL disorders is thought to be associated with lysosomal storage function.[provided by RefSeq, Oct 2008],
Gene Name: CLN5
Protein Name: Ceroid-lipofuscinosis neuronal protein 5
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分子量
- 46 kDa
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基因ID
- 1203
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OMIM
- 256731
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UniProt
- O75503
抗原
-
