Cannflavin A 可从大麻 (Cannabis sativa L.) 中分离得到。Cannflavin A 具有抗癌、神经保护和抗炎活性。Cannflavin A 可抑制 Aβ1-42 聚集。Cannflavin A 还能抑制犬尿氨酸-3-单加氧酶 (KMO) (IC50 = 29.4 μM)。Cannflavin A 通过 caspase-3 裂解激活细胞凋亡。Cannflavin A 通过抑制促炎酶 (包括 PC12 细胞系中的前列腺素 E2 和细胞色素 c 氧化酶 I 和 II) 发挥抗炎作用。
Ganoleucoin R 是一种可以从 Ganoderma leucocontextum 中分离得到的三萜类化合物。Ganoleucoin R 对 H2O2 诱导的氧化损伤具有保护作用,也能促进 PC12 细胞神经突生长。Ganoleucoin R 具有神经保护和促神经发生的活性,可用于神经退行性疾病的研究。
Cannflavin A (Standard) 是 Cannflavin A 的分析标准品。本产品用于研究及分析应用。Cannflavin A 可从大麻 (Cannabis sativa L.) 中分离得到。Cannflavin A 具有抗癌、神经保护和抗炎活性。Cannflavin A 可抑制 Aβ1-42 聚集。Cannflavin A 还能抑制犬尿氨酸-3-单加氧酶 (KMO) (IC50 = 29.4 μM)。Cannflavin A 通过 caspase-3 裂解激活细胞凋亡。Cannflavin A 通过抑制促炎酶 (包括 PC12 细胞系中的前列腺素 E2 和细胞色素 c 氧化酶 I 和 II) 发挥抗炎作用。
地黄甙 A
Rehmannioside A 是一种可以从 Rehmanniae radix 分离得到的化合物。Rehmannioside A 是 CYP3A4、2C9 和 2D6 的抑制剂,IC50 分别为 10.08、12.62 和 16.43 μM。Rehmannioside A 具有抗炎抗氧化、抗凋亡 (apoptosis)、抗铁死亡 (ferroptosis)、改善认识和神经保护的活性。Rehmannioside A 可用于神经系统和炎症相关疾病的研究。
积雪草苷 B
Asiaticoside B 是一种 9,19-环阿尔廷烷型三萜糖苷。Asiaticoside B 可诱导肝癌和乳腺癌细胞产生细胞毒性。Asiaticoside B 可减轻 6-OHDA (HY-B1081) 诱导的神经细胞损伤。Asiaticoside B 可用于肝癌、乳腺癌和帕金森病的相关研究。
Ginsenoside Ia 是一种三萜皂苷类化合物。Ginsenoside Ia 可通过抗氧化和凋亡通路发挥神经保护作用。Ginsenoside Ia 可缓解 H2O2 诱导的神经元损伤、降低 ROS 水平、抑制细胞凋亡 (apoptosis) 并稳定线粒体。Ginsenoside Ia 可用于神经退行性疾病的研究。
地黄甙 A
Rehmannioside A 是一种可以从 Rehmanniae radix 分离得到的化合物。Rehmannioside A 是 CYP3A4、2C9 和 2D6 的抑制剂,IC50 分别为 10.08、12.62 和 16.43 μM。Rehmannioside A 具有抗炎抗氧化、抗凋亡 (apoptosis)、抗铁死亡 (ferroptosis)、改善认识和神经保护的活性。Rehmannioside A 可用于神经系统和炎症相关疾病的研究。
Cannflavin A 可从大麻 (Cannabis sativa L.) 中分离得到。Cannflavin A 具有抗癌、神经保护和抗炎活性。Cannflavin A 可抑制 Aβ1-42 聚集。Cannflavin A 还能抑制犬尿氨酸-3-单加氧酶 (KMO) (IC50 = 29.4 μM)。Cannflavin A 通过 caspase-3 裂解激活细胞凋亡。Cannflavin A 通过抑制促炎酶 (包括 PC12 细胞系中的前列腺素 E2 和细胞色素 c 氧化酶 I 和 II) 发挥抗炎作用。
积雪草苷 B
Asiaticoside B 是一种 9,19-环阿尔廷烷型三萜糖苷。Asiaticoside B 可诱导肝癌和乳腺癌细胞产生细胞毒性。Asiaticoside B 可减轻 6-OHDA (HY-B1081) 诱导的神经细胞损伤。Asiaticoside B 可用于肝癌、乳腺癌和帕金森病的相关研究。
Ganoleucoin R 是一种可以从 Ganoderma leucocontextum 中分离得到的三萜类化合物。Ganoleucoin R 对 H2O2 诱导的氧化损伤具有保护作用,也能促进 PC12 细胞神经突生长。Ganoleucoin R 具有神经保护和促神经发生的活性,可用于神经退行性疾病的研究。
Cannflavin A (Standard) 是 Cannflavin A 的分析标准品。本产品用于研究及分析应用。Cannflavin A 可从大麻 (Cannabis sativa L.) 中分离得到。Cannflavin A 具有抗癌、神经保护和抗炎活性。Cannflavin A 可抑制 Aβ1-42 聚集。Cannflavin A 还能抑制犬尿氨酸-3-单加氧酶 (KMO) (IC50 = 29.4 μM)。Cannflavin A 通过 caspase-3 裂解激活细胞凋亡。Cannflavin A 通过抑制促炎酶 (包括 PC12 细胞系中的前列腺素 E2 和细胞色素 c 氧化酶 I 和 II) 发挥抗炎作用。
Ginsenoside Ia 是一种三萜皂苷类化合物。Ginsenoside Ia 可通过抗氧化和凋亡通路发挥神经保护作用。Ginsenoside Ia 可缓解 H2O2 诱导的神经元损伤、降低 ROS 水平、抑制细胞凋亡 (apoptosis) 并稳定线粒体。Ginsenoside Ia 可用于神经退行性疾病的研究。
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.