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~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～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。
Bisphenol A bis(3-chloro-2-hydroxypropyl) ether是一种有机化合物，具有潜在的抗菌活性。Bisphenol A bis(3-chloro-2-hydroxypropyl) ether可广泛应用于涂料和塑料制造，提升材料的强度与耐用性。Bisphenol A bis(3-chloro-2-hydroxypropyl) ether在纺织品处理过程中也发挥着重要作用，能够提高织物的抗皱和耐磨性能。
鱼明胶,suitable for cell culture
Fish Gelatin,suitable for cell culture 是一种天然生物聚合物。Fish Gelatin,suitable for cell culture 可从鱼类加工副产物中分离得到，例如鱼皮、鱼鳞、鱼骨和鱼鳔。Fish Gelatin,suitable for cell culture 已被认为是哺乳动物明胶的可行替代品。经修饰的 Fish Gelatin 在纳米材料、3D 打印、薄膜、涂层和生物制剂等多个行业中显示出巨大应用前景。Fish Gelatin,suitable for cell culture 适用于细胞培养，可用于细胞培养实验。
苯胺黑
Solvent black 5 (Spirit nigrosine) 是一种属于偶氮染料家族的合成染料。又称油黑或萘酚黑，呈深蓝黑色，在有机溶剂中溶解性极佳。Solvent black 5 通常用作印刷油墨、涂料和塑料等各种工业应用中的着色剂。它还可以用作检测溶液中金属存在的指示剂染料。此外，由于其在近红外区域的高吸收和发射特性，它已在科学研究中用作组织和细胞的荧光生物标志物。然而，据报道，Solvent black 5 对人类健康和环境具有潜在的毒性作用，因此在一些国家/地区对其使用进行了管制。
Bisphenol A bis(3-chloro-2-hydroxypropyl) ether-d14 是氘代标记的 Bisphenol A bis(3-chloro-2-hydroxypropyl) ether。Bisphenol A bis(3-chloro-2-hydroxypropyl) ether是一种有机化合物，具有潜在的抗菌活性。Bisphenol A bis(3-chloro-2-hydroxypropyl) ether可广泛应用于涂料和塑料制造，提升材料的强度与耐用性。Bisphenol A bis(3-chloro-2-hydroxypropyl) ether在纺织品处理过程中也发挥着重要作用，能够提高织物的抗皱和耐磨性能。
苯胺黑
Solvent black 5 (Spirit nigrosine) 是一种属于偶氮染料家族的合成染料。又称油黑或萘酚黑，呈深蓝黑色，在有机溶剂中溶解性极佳。Solvent black 5 通常用作印刷油墨、涂料和塑料等各种工业应用中的着色剂。它还可以用作检测溶液中金属存在的指示剂染料。此外，由于其在近红外区域的高吸收和发射特性，它已在科学研究中用作组织和细胞的荧光生物标志物。然而，据报道，Solvent black 5 对人类健康和环境具有潜在的毒性作用，因此在一些国家/地区对其使用进行了管制。
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。
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。
鱼明胶,suitable for cell culture
Fish Gelatin,suitable for cell culture 是一种天然生物聚合物。Fish Gelatin,suitable for cell culture 可从鱼类加工副产物中分离得到，例如鱼皮、鱼鳞、鱼骨和鱼鳔。Fish Gelatin,suitable for cell culture 已被认为是哺乳动物明胶的可行替代品。经修饰的 Fish Gelatin 在纳米材料、3D 打印、薄膜、涂层和生物制剂等多个行业中显示出巨大应用前景。Fish Gelatin,suitable for cell culture 适用于细胞培养，可用于细胞培养实验。
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～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。
Bisphenol A bis(3-chloro-2-hydroxypropyl) ether-d14 是氘代标记的 Bisphenol A bis(3-chloro-2-hydroxypropyl) ether。Bisphenol A bis(3-chloro-2-hydroxypropyl) ether是一种有机化合物，具有潜在的抗菌活性。Bisphenol A bis(3-chloro-2-hydroxypropyl) ether可广泛应用于涂料和塑料制造，提升材料的强度与耐用性。Bisphenol A bis(3-chloro-2-hydroxypropyl) ether在纺织品处理过程中也发挥着重要作用，能够提高织物的抗皱和耐磨性能。
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.
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