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Phospho-GFAP (Ser38) Antibody
具体的参考文献 (1) RMB 10000(报价是含税价格)
Description：Rabbit polyclonal antibody to Phospho-GFAP (Ser38)
Application：WB IHC IF/ICC
Reactivity：Phospho-GFAP (Ser38) Antibody detects endogenous levels of GFAP only when phosphorylated at Serine 38.
Conjugate：Human, Mouse, Rat
Isotype：Rabbit
产品名称
Phospho-GFAP (Ser38) Antibody
宿主
Rabbit
特异性
Phospho-GFAP (Ser38) Antibody detects endogenous levels of GFAP only when phosphorylated at Serine 38.
经测试应用
适用于:WB IHC IF/ICC
种属反应性
与反应:Human, Mouse, Rat
预测可用于: Bovine, Horse
预测可用于: Bovine, Horse
保存
Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
描述
This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. An additional transcript variant has been described, but its full length sequence has not been determined.
产品名称
Phospho-GFAP (Ser38) Antibody
宿主
Rabbit
特异性
Phospho-GFAP (Ser38) Antibody detects endogenous levels of GFAP only when phosphorylated at Serine 38.
经测试应用
适用于:WB IHC IF/ICC
种属反应性
与反应:Human, Mouse, Rat
预测可用于: Bovine, Horse
预测可用于: Bovine, Horse
保存
Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
描述
This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. An additional transcript variant has been described, but its full length sequence has not been determined.
产品名称
Phospho-GFAP (Ser38) Antibody
宿主
Rabbit
特异性
Phospho-GFAP (Ser38) Antibody detects endogenous levels of GFAP only when phosphorylated at Serine 38.
经测试应用
适用于:WB IHC IF/ICC
种属反应性
与反应:Human, Mouse, Rat
预测可用于: Bovine, Horse
预测可用于: Bovine, Horse
保存
Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
描述
This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. An additional transcript variant has been described, but its full length sequence has not been determined.
产品名称
Phospho-GFAP (Ser38) Antibody
宿主
Rabbit
特异性
Phospho-GFAP (Ser38) Antibody detects endogenous levels of GFAP only when phosphorylated at Serine 38.
经测试应用
适用于:WB IHC IF/ICC
种属反应性
与反应:Human, Mouse, Rat
预测可用于: Bovine, Horse
预测可用于: Bovine, Horse
保存
Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
描述
This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. An additional transcript variant has been described, but its full length sequence has not been determined.
产品名称
Phospho-GFAP (Ser38) Antibody
宿主
Rabbit
特异性
Phospho-GFAP (Ser38) Antibody detects endogenous levels of GFAP only when phosphorylated at Serine 38.
经测试应用
适用于:WB IHC IF/ICC
种属反应性
与反应:Human, Mouse, Rat
预测可用于: Bovine, Horse
预测可用于: Bovine, Horse
保存
Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
描述
This gene encodes one of the major intermediate filament proteins of mature astrocytes. It is used as a marker to distinguish astrocytes from other glial cells during development. Mutations in this gene cause Alexander disease, a rare disorder of astrocytes in the central nervous system. An additional transcript variant has been described, but its full length sequence has not been determined.
