LSMEM1 抗体 (AA 31-100) (HRP)
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- 抗原 See all LSMEM1 (C7ORF53) 抗体
- LSMEM1 (C7ORF53) (Chromosome 7 Open Reading Frame 53 (C7ORF53))
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抗原表位
- AA 31-100
- 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 LSMEM1 antibody is conjugated to HRP
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应用范围
- ELISA, Western Blotting (WB), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 预测反应
- Human,Mouse,Rat,Dog
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C7orf53
- 亚型
- IgG
- Top Product
- Discover our top product C7ORF53 Primary Antibody
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anti-Chromosome 7 Open Reading Frame 53 (C7ORF53) (AA 1-131) antibody
C7ORF53 适用: 人 ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
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- 应用备注
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WB 1:300-5000
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
- LSMEM1 (C7ORF53) (Chromosome 7 Open Reading Frame 53 (C7ORF53))
- 别名
- C7orf53 (C7ORF53 产品)
- 别名
- C7orf53 antibody, Gm889 antibody, C4H7orf53 antibody, C1H7orf53 antibody, C7ORF53 antibody, leucine rich single-pass membrane protein 1 antibody, leucine-rich single-pass membrane protein 1 antibody, LSMEM1 antibody, Lsmem1 antibody
- 背景
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Synonyms: C7orf53, CG053_HUMAN, Chromosome 7 open reading frame 53, Coiled-coil domain-containing transmembrane protein C7orf53.
Background: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf53 gene product has been provisionally designated C7orf53 pending further characterization.
- 基因ID
- 286006
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