SLAIN1 抗体 (AA 1-100) (AbBy Fluor® 555)
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- 抗原 See all SLAIN1 products
- SLAIN1 (SLAIN Motif Family, Member 1 (SLAIN1))
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抗原表位
- AA 1-100
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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 SLAIN1 antibody is conjugated to AbBy Fluor® 555
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应用范围
- Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 预测反应
- Human,Mouse,Rat,Dog,Chicken,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human SLAIN1/C13orf32
- 亚型
- IgG
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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
- SLAIN1 (SLAIN Motif Family, Member 1 (SLAIN1))
- 别名
- SLAIN1 (SLAIN1 产品)
- 别名
- 9630044O09Rik antibody, AA675320 antibody, AW742596 antibody, C13orf32 antibody, RGD1308626 antibody, zgc:175146 antibody, SLAIN motif family member 1 antibody, SLAIN motif family, member 1 antibody, SLAIN motif family, member 1b antibody, SLAIN1 antibody, Slain1 antibody, slain1b antibody
- 背景
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Synonyms: C13orf32, chromosome 13 open reading frame 32, FLJ30046, MGC131899, SLAI1_HUMAN, SLAIN mot family member 1, SLAIN mot family, member 1, SLAIN mot-containing protein 1, Slain1.
Background: SLAIN1 is a 561 amino acid member of the SLAIN motif-containing family and is expressed in embryonic stem cells, as well as in lung, brain and testis, where it exists as two alternatively spliced isoforms. The gene encoding SLAIN1 maps to human chromosome 13, which houses over 400 genes, such as BRCA2 and RB1, and comprises nearly 4 % of the human genome. As with most chromosomes, polysomy of part or all of chromosome 13 is deleterious to development and decreases the odds of survival. Trisomy 13, also known as Patau syndrome, is deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections.
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