ATRAID 抗体
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- 抗原 See all ATRAID 抗体
- ATRAID (All-Trans Retinoic Acid-Induced Differentiation Factor (ATRAID))
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适用
- 人, 大鼠, 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 ATRAID antibody is un-conjugated
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应用范围
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 人, 小鼠, 大鼠
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C2orf28
- 亚型
- IgG
- Top Product
- Discover our top product ATRAID Primary Antibody
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- 应用备注
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WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 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
- ATRAID (All-Trans Retinoic Acid-Induced Differentiation Factor (ATRAID))
- 别名
- C2orf28 (ATRAID 产品)
- 别名
- 0610007C21Rik antibody, AI316792 antibody, Apr3 antibody, HSPC013 antibody, p18 antibody, apr-3 antibody, apr3 antibody, c2orf28 antibody, APR--3 antibody, APR-3 antibody, APR3 antibody, C2orf28 antibody, PRO240 antibody, all-trans retinoic acid induced differentiation factor antibody, all-trans retinoic acid induced differentiation factor S homeolog antibody, all-trans retinoic acid-induced differentiation factor antibody, Atraid antibody, atraid.S antibody, ATRAID antibody, atraid antibody
- 背景
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Synonyms: Apoptosis related protein 3, Apoptosis related protein APR 3, APR 3, APR3, Chromosome 2 open reading frame 28, HSPC013, p18, PRO240, ARAID_HUMAN.
Background: APR3, also known as C2orf28 or p18, is a 229 amino acid single-pass membrane protein that contains one EGF-like domain and exists as two alternatively spliced isoforms. Expressed at a low level in hematopoietic cell lines, APR3 is thought to be involved in apoptosis and may also play a role in hematopoietic development and differentiation. The gene encoding APR3 maps to human chromosome 2, which houses over 1,400 genes and comprises nearly 8 % of the human genome. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene, while the lipid metabolic disorder sitosterolemia is associated with defects in the ABCG5 and ABCG8 genes. Additionally, an extremely rare recessive genetic disorder, Alstr syndrome, is caused by mutations in the ALMS1 gene, which maps to chromosome 2.
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