CLUAP1 抗体 (AA 35-140)
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- 抗原 See all CLUAP1 抗体
- CLUAP1 (Clusterin Associated Protein 1 (CLUAP1))
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抗原表位
- AA 35-140
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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 CLUAP1 antibody is un-conjugated
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应用范围
- ELISA, Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))
- 预测反应
- Human,Mouse,Rat,Dog,Sheep,Pig,Horse,Chicken,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human CLUAP1
- 亚型
- IgG
- Top Product
- Discover our top product CLUAP1 Primary Antibody
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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
- 浓度
- 1 μg/μL
- 缓冲液
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- 储存方法
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- 有效期
- 12 months
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- 抗原
- CLUAP1 (Clusterin Associated Protein 1 (CLUAP1))
- 别名
- CLUAP1 (CLUAP1 产品)
- 别名
- CLUAP1 antibody, MGC99254 antibody, FAP22 antibody, 2310030D15Rik antibody, 2610111M03Rik antibody, fj16b11 antibody, wu:fj16b11 antibody, zgc:56115 antibody, clusterin associated protein 1 antibody, clusterin associated protein 1 L homeolog antibody, CLUAP1 antibody, cluap1 antibody, cluap1.L antibody, Cluap1 antibody
- 背景
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Synonyms: Clusterin associated protein 1, FLJ13297, KIAA0643, CLUA1_HUMAN.
Background: CLUAP1 (Clusterin associated protein 1) is a 413 amino acid nuclear protein that exists as two alternatively spliced isoforms that interact with Clusterin. CLUAP1 is suggested to play a role in apoptosis and cell proliferation, and is expressed in testis, thrachea and thyroid, with low levels found in adrenal gland and spinal cord. The gene encoding CLUAP1 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, which is a gastrointestinal inflammatory condition.
- 基因ID
- 23059
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