Chromosome 5 Open Reading Frame 39 (C5orf39) (AA 50-100) 抗体 (Cy5)
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- 抗原 See all Chromosome 5 Open Reading Frame 39 (C5orf39) 抗体
- Chromosome 5 Open Reading Frame 39 (C5orf39)
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抗原表位
- AA 50-100
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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
- Cy5
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应用范围
- Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunofluorescence (Cultured Cells) (IF (cc))
- 预测反应
- Human
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human Annexin-2 receptor
- 亚型
- IgG
- Top Product
- Discover our top product C5orf39 Primary Antibody
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anti-Chromosome 5 Open Reading Frame 39 (C5orf39) (AA 1-193) antibody
C5orf39 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-Chromosome 5 Open Reading Frame 39 (C5orf39) (N-Term) antibodyC5orf39 适用: 人, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 5 Open Reading Frame 39 (C5orf39) (N-Term) antibodyC5orf39 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
- Chromosome 5 Open Reading Frame 39 (C5orf39)
- 别名
- AX2R (C5orf39 产品)
- 别名
- AX2R antibody, AXIIR antibody, C5orf39 antibody, annexin A2 receptor antibody, ANXA2R antibody
- 背景
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Synonyms: LOC389289, ANXA2R, Annexin 2 receptor, Annexin II receptor, AX2R, AXIIR, C5orf39, Chromosome 5 open reading frame 39, AX2R_HUMAN.
Background: ANXA2R (annexin-2 receptor), also known as AX2R or C5orf39, is a 193 amino acid protein that is widely expressed and may act as an annexin II receptor on marrow stromal cells to induce osteoclast formation. In addition, ANXA2R is highly expressed in lymphocytes and is also found in resting CD4+ and CD8+ T cells. The gene encoding ANXA2R maps to human chromosome 5, which contains 181 million base pairs and comprises nearly 6 % of the human genome. Chromosome 5 is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5-associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome, while deletion of the q arm or of chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.
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