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- 抗原 See all Occludin (OCLN) 抗体
- Occludin (OCLN)
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抗原表位
- AA 263-522
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适用
- 人
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宿主
- 兔
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克隆类型
- 多克隆
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标记
- This Occludin antibody is un-conjugated
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应用范围
- Western Blotting (WB)
- 序列
- FAVKTRRKMD RYDKSNILWD KEHIYDEQPP NVEEWVKNVS AGTQDVPSPP SDYVERVDSP MAYSSNGKVN DKRFYPESSY KSTPVPEVVQ ELPLTSPVDD FRQPRYSSGG NFETPSKRAP AKGRAGRSKR TEQDHYETDY TTGGESCDEL EEDWIREYPP ITSDQQRQLY KRNFDTGLQE YKSLQSELDE INKELSRLDK ELDDYREESE EYMAAADEYN RLKQVKGSAD YKSKKNHCKQ LKSKLSHIKK MVGDYDRQKT
- 交叉反应
- 人, 小鼠, 大鼠
- 产品特性
- Polyclonal Antibodies
- 免疫原
- Recombinant fusion protein containing a sequence corresponding to amino acids 263-522 of human Occludin (NP_002529.1).
- 亚型
- IgG
- Top Product
- Discover our top product OCLN Primary Antibody
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- 应用备注
- WB,1:1000 - 1:2000
- 说明
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HIGH QUALITY
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C. Avoid freeze / thaw cycles.
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The TRiC chaperonin controls reovirus replication through outer-capsid folding." in: Nature microbiology, Vol. 3, Issue 4, pp. 481-493, (2018) (PubMed).
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The TRiC chaperonin controls reovirus replication through outer-capsid folding." in: Nature microbiology, Vol. 3, Issue 4, pp. 481-493, (2018) (PubMed).
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- 抗原
- Occludin (OCLN)
- 别名
- OCLN (OCLN 产品)
- 别名
- AI503564 antibody, Ocl antibody, ocln antibody, oclnb antibody, tpmt antibody, OCLN antibody, wu:fd23h10 antibody, wu:fi13c01 antibody, zgc:113992 antibody, zgc:56359 antibody, BLCPMG antibody, occludin antibody, occludin S homeolog antibody, occludin a antibody, Ocln antibody, OCLN antibody, ocln.S antibody, ocln antibody, oclna antibody
- 背景
- This gene encodes an integral membrane protein that is required for cytokine-induced regulation of the tight junction paracellular permeability barrier. Mutations in this gene are thought to be a cause of band-like calcification with simplified gyration and polymicrogyria (BLC-PMG), an autosomal recessive neurologic disorder that is also known as pseudo-TORCH syndrome. Alternative splicing results in multiple transcript variants. A related pseudogene is present 1.5 Mb downstream on the q arm of chromosome 5.,OCLN,BLCPMG,PPP1R115,PTORCH1,occludin,Occludin,Signal Transduction,Cell Biology & Developmental Biology,Apoptosis,Cell Adhesion,Tight Junctions,Cytoskeleton,OCLN
- 分子量
- 8 kDa/23 kDa/31 kDa/52 kDa/54 kDa/59 kDa
- 基因ID
- 100506658
- UniProt
- Q16625
- 途径
- Cell-Cell Junction Organization, Hepatitis C
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