CLDND1 抗体 (AA 201-253)
Quick Overview for CLDND1 抗体 (AA 201-253) (ABIN719906)
抗原
See all CLDND1 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 201-253
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交叉反应
- 人
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预测反应
- Mouse,Rat,Dog,Cow,Sheep,Horse
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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 CLDND1
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亚型
- IgG
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anti-Claudin Domain Containing 1 (CLDND1) antibody
CLDND1 适用: 人, 小鼠 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Claudin Domain Containing 1 (CLDND1) (AA 26-140) antibodyCLDND1 适用: 人 ELISA, IF 宿主: 兔 Polyclonal unconjugated
anti-Claudin Domain Containing 1 (CLDND1) (AA 110-159) antibodyCLDND1 适用: 人, 小鼠, 大鼠, 犬, 马, Pig, 兔, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Claudin Domain Containing 1 (CLDND1) (Middle Region) antibodyCLDND1 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
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WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
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
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
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储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
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有效期
- 12 months
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- CLDND1 (Claudin Domain Containing 1 (CLDND1))
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别名
- CLDND1
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背景
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Synonyms: C3orf4, Chromosome 3 open reading frame 4, Claudin domain containing 1, Claudin domain containing 1 protein, Membrane protein GENX3745, CLDN1_HUMAN.
Background: CLDND1 is a 253 amino acid multi-pass membrane protein that is expressed at high levels in adult brain and at lower levels in adult heart. Existing as two alternatively spliced isoforms, CLDND1 is encoded by a gene that maps to human chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. 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
- 56650
抗原
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