ALDOA 抗体 (AA 50-364) (HRP)
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北京 101111
Quick Overview for ALDOA 抗体 (AA 50-364) (HRP) (ABIN7967668)
抗原
See all ALDOA 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- AA 50-364
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原理
- Anti-Aldolase/ALDOA Antibody HRP Conjugated
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特异性
- No cross reactivity with other proteins.
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交叉反应 (详细)
- No cross-reactivity with other proteins.
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纯化方法
- Immunogen affinity purified.
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免疫原
- E.coli-derived human Aldolase/ALDOA recombinant protein (Position: E50-Y364).
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亚型
- IgG
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应用备注
- Western blot, Optimal dilutions should be determined by end users. Immunohistochemistry (Paraffin-embedded Section), Optimal dilutions should be determined by end users. ELISA, Optimal dilutions should be determined by end users.
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限制
- 仅限研究用
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状态
- Liquid
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缓冲液
- Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4.
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储存条件
- -20 °C
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储存方法
- At -20°C for one year from date of receipt. Avoid repeated freezing and thawing.
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有效期
- 12 months
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- ALDOA (Aldolase A, Fructose-Bisphosphate (ALDOA))
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别名
- ALDOA
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背景
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Background: Aldolase A (ALDOA, or ALDA), also known as fructose-bisphosphate aldolase, is an enzyme that in humans is encoded by the ALDOA gene on chromosome 16. This gene encodes a member of the class I fructose-bisphosphate aldolase protein family. The encoded protein 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. Mutations in this gene have been associated with Glycogen Storage Disease XII, an autosomal recessive disorder associated with hemolytic anemia. Disruption of this gene also plays a role in the progression of multiple types of cancers. Related pseudogenes have been identified on chromosomes 3 and 10.
Gene Full Name: aldolase, fructose-bisphosphate A
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基因ID
- 226
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UniProt
- P04075
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途径
- Ribonucleoside Biosynthetic Process
抗原
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