FAM221A 抗体 (AA 201-298) (Alexa Fluor 350)
FAM221A
适用: 人
WB, IF (cc), IF (p)
宿主: 兔
Polyclonal
Alexa Fluor 350
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- 抗原 See all FAM221A 抗体
- FAM221A (Family with Sequence Similarity 221, Member A (FAM221A))
- 抗原表位
- AA 201-298
- 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 FAM221A antibody is conjugated to Alexa Fluor 350
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应用范围
- Western Blotting (WB), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- 交叉反应
- 人
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C7orf46
- 亚型
- IgG
- Top Product
- Discover our top product FAM221A Primary Antibody
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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
- FAM221A (Family with Sequence Similarity 221, Member A (FAM221A))
- 别名
- C7orf46 (FAM221A 产品)
- 别名
- C7orf46 antibody, D330028D13Rik antibody, c7orf46 antibody, family with sequence similarity 221 member A antibody, family with sequence similarity 221, member A antibody, family with sequence similarity 221 member A L homeolog antibody, FAM221A antibody, Fam221a antibody, fam221a.L antibody
- 背景
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Synonyms: C7orf46, F221A_HUMAN, Chromosome 7 open reading frame 46, Uncharacterized protein C7orf46.
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 C7orf46 gene product has been provisionally designated C7orf46 pending further characterization.
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