C7orf42 抗体 (AA 231-314) (Biotin)
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- 抗原 See all C7orf42 products
- C7orf42 (Chromosome 7 Open Reading Frame 42 (C7orf42))
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抗原表位
- AA 231-314
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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 C7orf42 antibody is conjugated to Biotin
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应用范围
- Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- 预测反应
- Human,Mouse,Rat,Dog,Cow,Sheep,Pig,Horse,Chicken,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C7orf42
- 亚型
- IgG
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anti-Chromosome 7 Open Reading Frame 42 (C7orf42) antibody
C7orf42 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 7 Open Reading Frame 42 (C7orf42) (N-Term) antibodyC7orf42 适用: 人, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 7 Open Reading Frame 42 (C7orf42) (N-Term) antibodyC7orf42 适用: 人 WB 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.
- 储存条件
- -20 °C
- 储存方法
- Store at -20°C for 12 months.
- 有效期
- 12 months
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- 抗原
- C7orf42 (Chromosome 7 Open Reading Frame 42 (C7orf42))
- 别名
- C7orf42 (C7orf42 产品)
- 别名
- C7orf42 antibody, c7orf42 antibody, TMEM248 antibody, MGC79534 antibody, C25H7orf42 antibody, 0610007L01Rik antibody, A930023A16Rik antibody, AW557951 antibody, G430067H08Rik antibody, zgc:103561 antibody, transmembrane protein 248 antibody, transmembrane protein 248 L homeolog antibody, TMEM248 antibody, tmem248.L antibody, tmem248 antibody, Tmem248 antibody
- 背景
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Synonyms: C7orf42, TM248_HUMAN, Chromosome 7 open reading frame 42, FLJ10099, FLJ13090, Hypothetical protein LOC55069, UPF0458 protein C7orf42.
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 C7orf42 gene product has been provisionally designated C7orf42 pending further characterization.
- 基因ID
- 55069
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