Toluidine Blue (Toluidine Blue O) purity 36% 是一种碱性的醌亚胺染料 (活体染料)，对酸性组织成分有很高的亲和力，可将细胞核染成蓝色，多糖染成紫色。Toluidine Blue purity 36% 对肥大细胞、粘蛋白和软骨细胞显示异染性。Toluidine Blue purity 36% 可使植物组织和细胞的不同成分染成不同的颜色。Toluidine Blue purity 36% 还可作为辅助诊断工具，鉴别恶性病变，如癌症。
Ladyginoside A 是一种三萜皂苷，被发现存在于南洋参 (Polyscias fruticosa (L.) Harms) 的叶子中。Ladyginoside A 对 α-淀粉酶 (α-amylase) 和 α-葡萄糖苷酶 (α-glucosidase) 具有抑制活性，能够调节碳水化合物代谢。Ladyginoside A 还表现出潜在的抗炎和肥大细胞稳定作用。Ladyginoside A 可用于炎症和代谢性疾病的研究，如糖尿病。
甲苯胺蓝O
Toluidine Blue (Toluidine Blue O) 是一种碱性的醌亚胺染料 (活体染料)，对酸性组织成分有很高的亲和力，可将细胞核染成蓝色，多糖染成紫色。Toluidine Blue 对肥大细胞、粘蛋白和软骨细胞显示异染性。Toluidine Blue 可使植物组织和细胞的不同成分染成不同的颜色。Toluidine Blue 还可作为辅助诊断工具，鉴别恶性病变，如癌症。
甲苯胺兰
Toluidine blue (ZnCl2) 是一种碱性噻嗪染料，通常用作显微镜检查的生物染色剂。它具有深蓝紫色，常用于对 DNA 和 RNA 等核酸进行染色，以及对肥大细胞、软骨和其他结缔组织进行染色。Toluidine blue (ZnCl2) 染色这些组织的酸性成分，例如硫酸化或羧化粘多糖。它经常用于组织学、细胞学和病理学应用，以帮助诊断各种疾病和病症。染料通常在显微镜检查之前应用于组织切片，并且可以使用酸性酒精溶液进行区分。Toluidine blue (ZnCl2) 是一种相对简单且廉价的染色剂，具有良好的重现性，使其成为许多实验室的流行选择。
Toluidine Blue (Toluidine Blue O) purity 36% 是一种碱性的醌亚胺染料 (活体染料)，对酸性组织成分有很高的亲和力，可将细胞核染成蓝色，多糖染成紫色。Toluidine Blue purity 36% 对肥大细胞、粘蛋白和软骨细胞显示异染性。Toluidine Blue purity 36% 可使植物组织和细胞的不同成分染成不同的颜色。Toluidine Blue purity 36% 还可作为辅助诊断工具，鉴别恶性病变，如癌症。
甲苯胺兰
Toluidine blue (ZnCl2) 是一种碱性噻嗪染料，通常用作显微镜检查的生物染色剂。它具有深蓝紫色，常用于对 DNA 和 RNA 等核酸进行染色，以及对肥大细胞、软骨和其他结缔组织进行染色。Toluidine blue (ZnCl2) 染色这些组织的酸性成分，例如硫酸化或羧化粘多糖。它经常用于组织学、细胞学和病理学应用，以帮助诊断各种疾病和病症。染料通常在显微镜检查之前应用于组织切片，并且可以使用酸性酒精溶液进行区分。Toluidine blue (ZnCl2) 是一种相对简单且廉价的染色剂，具有良好的重现性，使其成为许多实验室的流行选择。
Ladyginoside A 是一种三萜皂苷，被发现存在于南洋参 (Polyscias fruticosa (L.) Harms) 的叶子中。Ladyginoside A 对 α-淀粉酶 (α-amylase) 和 α-葡萄糖苷酶 (α-glucosidase) 具有抑制活性，能够调节碳水化合物代谢。Ladyginoside A 还表现出潜在的抗炎和肥大细胞稳定作用。Ladyginoside A 可用于炎症和代谢性疾病的研究，如糖尿病。
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.
![1,1′-Ethylidenebis[L-tryptophan]](http://hg.y866.cn/biomolecule/lib/file/product_pic/hy-w585843.gif)
