SHROOM1 抗体 (AA 121-220) (HRP)
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- 抗原 See all SHROOM1 抗体
- SHROOM1 (Shroom Family Member 1 (SHROOM1))
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抗原表位
- AA 121-220
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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 SHROOM1 antibody is conjugated to HRP
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应用范围
- ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 交叉反应
- 人
- 预测反应
- Mouse,Rat,Dog,Cow,Sheep
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human SHROOM1
- 亚型
- IgG
- Top Product
- Discover our top product SHROOM1 Primary Antibody
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- 应用备注
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IHC-P 1:200-400
IHC-F 1:100-500 - 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.
- 注意事项
- Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
- 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
- SHROOM1 (Shroom Family Member 1 (SHROOM1))
- 别名
- SHROOM1 (SHROOM1 产品)
- 别名
- apx antibody, APXL2 antibody, 1300007L22Rik antibody, Apx antibody, Shrm1 antibody, RGD1308066 antibody, shrm antibody, shroom family member 1 antibody, shroom family member 1 L homeolog antibody, SHROOM1 antibody, shroom1 antibody, Shroom1 antibody, shroom1.L antibody
- 背景
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Synonyms: Apical protein 2, APXL2, Protein Shroom1, SHRM1_HUMAN, Shroom family member 1, Shroom1.
Background: SHROOM1 is an 852 amino acid protein that contains one ASD1 domain and one ASD2 domain. Localized to both the cytoplasm and the cytoskeleton, SHROOM1 interacts with Actin and is thought to be involved in microtubule assembly during cell elongation, possibly playing a role in the development of the nervous system. Multiple isoforms of SHROOM1 exist due to alternative splicing events. The gene encoding SHROOM1 maps to human chromosome 5, which contains 181 million base pairs and comprises nearly 6 % of the human genome. 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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