HOXA6 抗体 (AA 171-233) (AbBy Fluor® 555)
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- 抗原 See all HOXA6 抗体
- HOXA6 (Homeobox A6 (HOXA6))
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抗原表位
- AA 171-233
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适用
- 人, 小鼠, 大鼠
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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 HOXA6 antibody is conjugated to AbBy Fluor® 555
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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, 小鼠, 大鼠
- 预测反应
- Dog,Sheep,Pig,Horse
- 纯化方法
- Purified by Protein A.
- 免疫原
- KLH conjugated synthetic peptide derived from human HOXA6/HOX1B
- 亚型
- IgG
- Top Product
- Discover our top product HOXA6 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
- HOXA6 (Homeobox A6 (HOXA6))
- 别名
- HOXA6/HOX1B (HOXA6 产品)
- 别名
- HOX1 antibody, HOX1.2 antibody, HOX1B antibody, Hox-1.2 antibody, homeobox A6 antibody, HOXA6 antibody, hoxa6 antibody, Hoxa6 antibody
- 背景
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Synonyms: Homeo box 1B, Homeo box A6, Homeobox 1B, Homeobox A6, Homeobox protein Hox A6, Homeobox protein Hox-1B, Homeobox protein Hox-A6 antibody Homeobox protein HoxA6, HOX 1, Hox 1B, HOX1, HOX1.2, Hox1B, HOXA6, HX A6, HXA6, HXA6_HUMAN.
Background: The Hox homeobox genes encode proteins that are transcriptional regulators with an established role in embryonic development. HoxA6 (homeobox A6), also known as HOX1B, is a 233 amino acid protein that localizes to the nucleus. Expressed during embryonic development, HoxA6 functions as a sequence-specific DNA-binding transcription factor that is part of a regulatory mechanism that provides cells with positional identities during development. Via its ability to bind DNA, HoxA6 plays an important role in the regulation of gene expression, as well as morphogenesis and differentiation. The gene encoding HoxA6 maps to human chromosome 7, which houses over 1,000 genes and comprises nearly 5 % of the human genome. Defects in some of the genes localized to chromosome 7 have been linked to Osteogenesis imperfecta, Williams-Beuren syndrome, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome.
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