GALE 抗体 (Middle Region)
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北京 101111
Quick Overview for GALE 抗体 (Middle Region) (ABIN928723)
抗原
See all GALE 抗体适用
宿主
克隆类型
标记
应用范围
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抗原表位
- Middle Region
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纯化方法
- Purified
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免疫原
- GALE antibody was raised in rabbit using the middle region of GALE as the immunogen
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anti-UDP-Galactose-4-Epimerase (GALE) antibody
GALE 适用: 人, 大鼠, 犬, 猴 WB, IHC, IHC (p) 宿主: 小鼠 Monoclonal 1C4 unconjugated
anti-UDP-Galactose-4-Epimerase (GALE) (AA 1-340) antibodyGALE 适用: 人, 小鼠, 大鼠 WB, ELISA, IHC 宿主: 兔 Polyclonal unconjugated
anti-UDP-Galactose-4-Epimerase (GALE) (AA 1-348) antibodyGALE 适用: 人 WB, ELISA, IHC, IF 宿主: 兔 Polyclonal unconjugated
anti-UDP-Galactose-4-Epimerase (GALE) (AA 142-171) antibodyGALE 适用: 人 WB, IF, IHC (p), FACS 宿主: 兔 Polyclonal RB21189 unconjugated
anti-UDP-Galactose-4-Epimerase (GALE) antibodyKD Validated GALE 适用: 人 WB, FACS 宿主: 小鼠 Monoclonal 24GB13050 unconjugated
anti-UDP-Galactose-4-Epimerase (GALE) (AA 1-348) antibodyGALE 适用: 人 WB, IP 宿主: 兔 Polyclonal unconjugated
anti-UDP-Galactose-4-Epimerase (GALE) (AA 1-348) antibodyGALE 适用: 人 WB 宿主: 小鼠 Polyclonal unconjugated
anti-UDP-Galactose-4-Epimerase (GALE) (AA 129-348) antibodyGALE 适用: 人 WB, IHC 宿主: 兔 Polyclonal unconjugated
anti-UDP-Galactose-4-Epimerase (GALE) (AA 1-348) antibodyGALE 适用: 人 WB, ELISA, IF, ICC 宿主: 小鼠 Monoclonal AT6G10 unconjugated
anti-UDP-Galactose-4-Epimerase (GALE) (N-Term) antibodyGALE 适用: 人 WB 宿主: 兔 Polyclonal unconjugated
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应用备注
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WB: 0.2-1 µg/mL
Optimal conditions should be determined by the investigator. -
说明
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GALE Blocking Peptide, (ABIN5613709), is also available for use as a blocking control in assays to test for specificity of this GALE antibody
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限制
- 仅限研究用
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状态
- Lyophilized
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浓度
- Lot specific
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缓冲液
- Lyophilized powder. Add 50 µL of distilled water. Final antibody concentration is 1 mg/mL in PBS buffer.
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注意事项
- Avoid repeated freeze/thaw cycles.
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储存条件
- 4 °C/-20 °C
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储存方法
- Store at 4 °C, following reconstitution, aliquot and store at -20 °C.
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- GALE (UDP-Galactose-4-Epimerase (GALE))
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别名
- GALE
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背景
- GALE is an UDP-galactose-4-epimerase which catalyzes two distinct but analogous reactions: the epimerization of UDP-glucose to UDP-galactose, and the epimerization of UDP-N-acetylglucosamine to UDP-N-acetylgalactosamine. The bifunctional nature of the enzyme has the important metabolic consequence that mutant cells (or individuals) are dependent not only on exogenous galactose, but also on exogenous N-acetylgalactosamine as a necessary precursor for the synthesis of glycoproteins and glycolipids. Mutations in this gene result in epimerase-deficiency galactosemia, also referred to as galactosemia type 3, a disease characterized by liver damage, early-onset cataracts, deafness and mental retardation, with symptoms ranging from mild to severe ('generalized' form). Synonyms: Polyclonal GALE antibody, Anti-GALE antibody, UDP-galactose-4-epimerase antibody.
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途径
- Response to Water Deprivation, Cellular Glucan Metabolic Process
抗原
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