DEXI 抗体 (AA 51-95) (Cy5)
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- 抗原 See all DEXI 抗体
- DEXI (Dexamethasone-Induced Transcript (DEXI))
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抗原表位
- AA 51-95
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适用
- 小鼠
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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 DEXI antibody is conjugated to Cy5
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应用范围
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 小鼠
- 预测反应
- Human,Rat,Cow,Sheep,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human DEXI
- 亚型
- IgG
- Top Product
- Discover our top product DEXI Primary Antibody
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anti-Dexamethasone-Induced Transcript (DEXI) (AA 1-95) antibody
DEXI 适用: 人 ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Dexamethasone-Induced Transcript (DEXI) (AA 1-95) antibodyDEXI 适用: 人 WB 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
- 浓度
- 1 μg/μL
- 缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- 储存液
- ProClin
- 注意事项
- This product contains ProClin: 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- 有效期
- 12 months
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- 抗原
- DEXI (Dexamethasone-Induced Transcript (DEXI))
- 别名
- DEXI (DEXI 产品)
- 别名
- 1810029J14Rik antibody, AI836170 antibody, AW413143 antibody, D16Bwg0586e antibody, Myle antibody, MYLE antibody, RGD1564938 antibody, zgc:101082 antibody, dexamethasone-induced transcript antibody, Dexi homolog antibody, Dexi homolog (mouse) antibody, Dexi antibody, DEXI antibody, dexi antibody
- 背景
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Synonyms: Dexamethasone-induced protein, DEXI, DEXI_HUMAN, MYLE, Protein MYLE.
Background: DEXI is a 95 amino acid protein belonging to the DEXI family. Induced by dexamethasone, DEXI is expressed in brain, liver, pancreas, placenta and lung, with highest levels in heart. DEXI is also up-regulated in emphysematous lung compared to normal lung. The gene encoding DEXI maps to human chromosome 16, which encodes over 900 genes and comprises nearly 3 % of the human genome. The GAN gene is located on chromosome 16 and, with mutation, may lead to giant axonal neuropathy, a nervous system disorder characterized by increasing malfunction with growth. The rare disorder Rubinstein-Taybi syndrome is also associated with chromosome 16, as is Crohn's disease, a gastrointestinal inflammatory condition.
- 基因ID
- 28955
- UniProt
- O95424
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