ALDOA 抗体 (AA 9-145)
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- 抗原 See all ALDOA 抗体
- ALDOA (Aldolase A, Fructose-Bisphosphate (ALDOA))
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抗原表位
- AA 9-145
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适用
- 人
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宿主
- 小鼠
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克隆类型
- 单克隆
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标记
- This ALDOA antibody is un-conjugated
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应用范围
- ELISA, Immunocytochemistry (ICC), Flow Cytometry (FACS)
- 原理
- ALDOA Antibody
- 纯化方法
- Purified antibody
- 免疫原
- Purified recombinant fragment of human ALDOA (AA: 9-145) expressed in E. Coli.
- 克隆位点
- 2H2B1
- 亚型
- IgG1
- Top Product
- Discover our top product ALDOA Primary Antibody
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- 应用备注
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ELISA: 1/10000
FCM: 1/200 - 1/400
ICC: 1/100 - 1/500
- 限制
- 仅限研究用
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- 状态
- Liquid
- 缓冲液
- Purified antibody in PBS with 0.05 % sodium azide.
- 储存液
- Sodium azide
- 注意事项
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- 储存条件
- 4 °C,-20 °C
- 储存方法
- Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
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- 抗原
- ALDOA (Aldolase A, Fructose-Bisphosphate (ALDOA))
- 别名
- ALDOA (ALDOA 产品)
- 别名
- ALDA antibody, GSD12 antibody, aldoa antibody, cb79 antibody, sb:cb79 antibody, wu:fa28b10 antibody, wu:fb10b11 antibody, ALDOA antibody, Aldo-1 antibody, Aldo1 antibody, RNALDOG5 antibody, hm:zeh0036 antibody, zgc:77696 antibody, aldolase, fructose-bisphosphate A antibody, aldolase a, fructose-bisphosphate, a antibody, aldolase, fructose-bisphosphate A S homeolog antibody, aldolase A, fructose-bisphosphate antibody, aldolase a, fructose-bisphosphate, b antibody, ALDOA antibody, aldoaa antibody, aldoa antibody, aldoa.S antibody, Aldoa antibody, aldoab antibody
- 背景
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Description: The protein encoded by this gene, Aldolase A (fructose-bisphosphate aldolase), is a glycolytic enzyme that catalyzes the reversible conversion of fructose-1,6-bisphosphate to glyceraldehyde 3-phosphate and dihydroxyacetone phosphate. Three aldolase isozymes (A, B, and C), encoded by three different genes, are differentially expressed during development. Aldolase A is found in the developing embryo and is produced in even greater amounts in adult muscle. Aldolase A expression is repressed in adult liver, kidney and intestine and similar to aldolase C levels in brain and other nervous tissue. Aldolase A deficiency has been associated with myopathy and hemolytic anemia. Alternative splicing and alternative promoter usage results in multiple transcript variants. Related pseudogenes have been identified on chromosomes 3 and 10.
Aliases: ALDA, GSD12, HEL-S-87p
- 分子量
- 39.4kDa
- 基因ID
- 226
- HGNC
- 226
- UniProt
- P04075
- 途径
- Ribonucleoside Biosynthetic Process
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