聚乙烯吡咯烷酮,average Mw~29000
Polyvinylpyrrolidone, average Mw~29000，是一种多功能合成聚合物，平均分子量为 29000 Da。Polyvinylpyrrolidone, average Mw~29000 是一种用途广泛的赋形剂，可用于传统制剂和新型控释或靶向递送系统，可用作粘合剂、包衣剂、悬浮剂、成孔剂、增溶剂、稳定剂等。
聚乙烯吡咯烷酮,average Mw~10000
Polyvinylpyrrolidone, average Mw~10000，是一种多功能合成聚合物，平均分子量为 10000 Da。Polyvinylpyrrolidone, average Mw~10000 被广泛用于纳米颗粒的合成。Polyvinylpyrrolidone, average Mw~10000 是一种用途广泛的赋形剂，可用于传统制剂和新型控释或靶向递送系统，可用作粘合剂、包衣剂、悬浮剂、成孔剂、增溶剂、稳定剂等。
聚乙烯吡咯烷酮,average Mw～55000
Polyvinylpyrrolidone, average Mw~55000，是一种多功能合成聚合物，平均分子量为 55000 Da。Polyvinylpyrrolidone, average Mw~55000 被广泛用于纳米颗粒的合成。Polyvinylpyrrolidone, average Mw~55000 是一种用途广泛的赋形剂，可用于传统制剂和新型控释或靶向递送系统，可用作粘合剂、包衣剂、悬浮剂、成孔剂、增溶剂、稳定剂等。
聚乙烯吡咯烷酮,average Mw～360000
Polyvinylpyrrolidone, average Mw~360000，是一种多功能合成聚合物，平均分子量为 360000 Da。Polyvinylpyrrolidone, average Mw~360000 被广泛用于纳米颗粒的合成。Polyvinylpyrrolidone, average Mw~360000 是一种用途广泛的赋形剂，可用于传统制剂和新型控释或靶向递送系统，可用作粘合剂、包衣剂、悬浮剂、成孔剂、增溶剂、稳定剂等。
聚乙烯吡咯烷酮,average Mw~40000
Polyvinylpyrrolidone, average Mw~40000，是一种多功能合成聚合物，平均分子量为 40000 Da。Polyvinylpyrrolidone, average Mw~40000 广泛用于合成纳米颗粒。Polyvinylpyrrolidone, average Mw~40000 是一种用途广泛的赋形剂，可用于传统制剂和新型控释或靶向递送系统，可用作粘合剂、包衣剂、悬浮剂、成孔剂、增溶剂、稳定剂等。
3-(Dimethyl(octadecyl)ammonio)propane-1-sulfonate 是季铵化合物类。它是一种具有两亲特性的表面活性剂和阳离子洗涤剂，因此可用于各种工业和生物医学应用。3-(二甲基(十八烷基)铵)丙烷-1-磺酸盐通常用作个人护理产品、清洁剂、纺织品和药物配方中的乳化剂、增溶剂和抗菌剂。它还用作分析化学中的试剂，特别是在蛋白质和 DNA 的分析中。
聚乙烯吡咯烷酮,average Mw~29000
Polyvinylpyrrolidone, average Mw~29000，是一种多功能合成聚合物，平均分子量为 29000 Da。Polyvinylpyrrolidone, average Mw~29000 是一种用途广泛的赋形剂，可用于传统制剂和新型控释或靶向递送系统，可用作粘合剂、包衣剂、悬浮剂、成孔剂、增溶剂、稳定剂等。
聚乙烯吡咯烷酮,average Mw~10000
Polyvinylpyrrolidone, average Mw~10000，是一种多功能合成聚合物，平均分子量为 10000 Da。Polyvinylpyrrolidone, average Mw~10000 被广泛用于纳米颗粒的合成。Polyvinylpyrrolidone, average Mw~10000 是一种用途广泛的赋形剂，可用于传统制剂和新型控释或靶向递送系统，可用作粘合剂、包衣剂、悬浮剂、成孔剂、增溶剂、稳定剂等。
聚乙烯吡咯烷酮,average Mw～360000
Polyvinylpyrrolidone, average Mw~360000，是一种多功能合成聚合物，平均分子量为 360000 Da。Polyvinylpyrrolidone, average Mw~360000 被广泛用于纳米颗粒的合成。Polyvinylpyrrolidone, average Mw~360000 是一种用途广泛的赋形剂，可用于传统制剂和新型控释或靶向递送系统，可用作粘合剂、包衣剂、悬浮剂、成孔剂、增溶剂、稳定剂等。
聚乙烯吡咯烷酮,average Mw～55000
Polyvinylpyrrolidone, average Mw~55000，是一种多功能合成聚合物，平均分子量为 55000 Da。Polyvinylpyrrolidone, average Mw~55000 被广泛用于纳米颗粒的合成。Polyvinylpyrrolidone, average Mw~55000 是一种用途广泛的赋形剂，可用于传统制剂和新型控释或靶向递送系统，可用作粘合剂、包衣剂、悬浮剂、成孔剂、增溶剂、稳定剂等。
聚乙烯吡咯烷酮,average Mw~40000
Polyvinylpyrrolidone, average Mw~40000，是一种多功能合成聚合物，平均分子量为 40000 Da。Polyvinylpyrrolidone, average Mw~40000 广泛用于合成纳米颗粒。Polyvinylpyrrolidone, average Mw~40000 是一种用途广泛的赋形剂，可用于传统制剂和新型控释或靶向递送系统，可用作粘合剂、包衣剂、悬浮剂、成孔剂、增溶剂、稳定剂等。
3-(Dimethyl(octadecyl)ammonio)propane-1-sulfonate 是季铵化合物类。它是一种具有两亲特性的表面活性剂和阳离子洗涤剂，因此可用于各种工业和生物医学应用。3-(二甲基(十八烷基)铵)丙烷-1-磺酸盐通常用作个人护理产品、清洁剂、纺织品和药物配方中的乳化剂、增溶剂和抗菌剂。它还用作分析化学中的试剂，特别是在蛋白质和 DNA 的分析中。
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
MedchemExpress Validation 03
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
MedchemExpress Validation 04
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
MedchemExpress Validation
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
MedchemExpress Validation
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
MedchemExpress Validation
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
MedchemExpress Validation
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
MedchemExpress Validation
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
MedchemExpress Validation
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
MedchemExpress Validation
Western blot analysis of extracts from THP-1(lane 2(20μg), Jurkat (lane 3(20μg) and NIH3T3(lane 4(20μg) using FOXO1A (HY-P80132) Rabbit mAb. Proteins were transferred
to a PVDF membrane and blocked with 5% non-fat milk in TBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (Beta Actin, HY-P80438, 1/10000) was
used in 5% non-fat milk in TBST at 4°C overnight. Goat Anti-Mouse/Rabbit IgG-HRP Secondary Antibody (1/10000) was used for 1 hour at room temperature.
