C7orf64 抗体 (AA 1-100) (Alexa Fluor 350)
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- 抗原 See all C7orf64 抗体
- C7orf64 (Chromosome 7 Open Reading Frame 64 (C7orf64))
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抗原表位
- AA 1-100
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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
- This C7orf64 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
- 预测反应
- Mouse,Rat,Dog,Cow,Sheep,Horse,Chicken,Rabbit
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human C7orf64
- 亚型
- IgG
- Top Product
- Discover our top product C7orf64 Primary Antibody
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anti-Chromosome 7 Open Reading Frame 64 (C7orf64) (AA 1-100) antibody
C7orf64 适用: 人 WB, IF (cc), IF (p), ELISA, IHC (p), IHC (fro), ICC 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 7 Open Reading Frame 64 (C7orf64) (AA 42-91) antibodyC7orf64 适用: 人, 小鼠, 犬, 马, Pig, 大鼠, Cow, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Chromosome 7 Open Reading Frame 64 (C7orf64) (AA 297-346) antibodyC7orf64 适用: 人, 小鼠 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
- C7orf64 (Chromosome 7 Open Reading Frame 64 (C7orf64))
- 别名
- C7orf64 (C7orf64 产品)
- 别名
- C7orf64 antibody, DKFZP564O0523 antibody, HSPC304 antibody, RGD1310794 antibody, AW548102 antibody, C030048B08Rik antibody, dkfzp564o0523 antibody, C4H7orf64 antibody, RNA binding motif protein 48 antibody, rbm48 antibody, RBM48 antibody, Rbm48 antibody
- 背景
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Synonyms: C7orf64, RBM48_HUMAN, DKFZP564O0523, DKFZp686D1651, HSPC304, Hypothetical protein LOC84060, OTTHUMP00000215752, UPF0712 protein C7orf64.
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 C7orf64 gene product has been provisionally designated C7orf64 pending further characterization.
- 基因ID
- 84060
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