Prussian blue insoluble (Standard) 是 Prussian blue insoluble (HY-106594A) 的分析标准品。本产品用于研究及分析应用。Prussian blue soluble 是一种很好的吸附剂，可用作铯或铊离子中毒的解毒剂。Prussian blue soluble 具有抗癌和抗菌特性。Prussian blue soluble 可作为光声和磁共振成像 (MRI) 中的造影剂。
普鲁士蓝可溶 (标准品)
Prussian blue soluble (Standard) 是 Prussian blue soluble (HY-106594B) 的分析标准品。本产品用于研究及分析应用。Prussian blue soluble 是一种很好的吸附剂，可用作铯或铊离子中毒的解毒剂。Prussian blue soluble 具有抗癌和抗菌特性。Prussian blue soluble 可作为光声和磁共振成像 (MRI) 中的造影剂。
Diatrizoic acid EP impurity A是一种有机化合物，具有对生物系统的潜在影响和特定药理活性。Diatrizoic acid EP impurity A可被用于影像学检查中的造影剂以增强X光、CT扫描等影像的清晰度。Diatrizoic acid EP impurity A也被研究用于化合物的分离和分析。
NIR-RED ATP Probe 是一种 NIR-II 荧光探针。NIR-RED ATP Probe 对 ATP 表现出高亲和力和选择性，可在活体水平高对比度、无创地检测 ATP 的浓度变化，而对细胞内丰富的生物分子干扰很小。NIR-RED ATP Probe 可用于药物性肝损伤 (DILI) 的生物标志物检测工具。
偶氮氯膦 III
Chlorophosphonazo III 是一种可透过细胞膜的造影剂和分光光度试剂。Chlorophosphonazo III 可与细胞内的钙、镁、铀、钛、锆、钍、钪、等价锕系元素及镤形成 1:1 的稳定复合物。Chlorophosphonazo III 可产生与 Ca2+ 浓度相关的光声信号，用于 3D 肿瘤细胞培养物和肿瘤球的成像。Chlorophosphonazo III 无细胞毒性，可用于目标离子的分光光度检测，且在 pH 2.2 至 7.0 的范围内，其复合物吸光度可稳定维持长达一周。
丙氨酸 (标准品)
L-Alanine (Standard) 是 L-Alanine 的分析标准品。本产品用于研究及分析应用。L-Alanine is a non-essential amino acid, involved in sugar and acid metabolism, increases immunity, and provides energy for muscle tissue, brain, and central nervous system.
NIR-RED ATP Probe 是一种 NIR-II 荧光探针。NIR-RED ATP Probe 对 ATP 表现出高亲和力和选择性，可在活体水平高对比度、无创地检测 ATP 的浓度变化，而对细胞内丰富的生物分子干扰很小。NIR-RED ATP Probe 可用于药物性肝损伤 (DILI) 的生物标志物检测工具。
普鲁士蓝可溶 (标准品)
Prussian blue soluble (Standard) 是 Prussian blue soluble (HY-106594B) 的分析标准品。本产品用于研究及分析应用。Prussian blue soluble 是一种很好的吸附剂，可用作铯或铊离子中毒的解毒剂。Prussian blue soluble 具有抗癌和抗菌特性。Prussian blue soluble 可作为光声和磁共振成像 (MRI) 中的造影剂。
偶氮氯膦 III
Chlorophosphonazo III 是一种可透过细胞膜的造影剂和分光光度试剂。Chlorophosphonazo III 可与细胞内的钙、镁、铀、钛、锆、钍、钪、等价锕系元素及镤形成 1:1 的稳定复合物。Chlorophosphonazo III 可产生与 Ca2+ 浓度相关的光声信号，用于 3D 肿瘤细胞培养物和肿瘤球的成像。Chlorophosphonazo III 无细胞毒性，可用于目标离子的分光光度检测，且在 pH 2.2 至 7.0 的范围内，其复合物吸光度可稳定维持长达一周。
丙氨酸 (标准品)
L-Alanine (Standard) 是 L-Alanine 的分析标准品。本产品用于研究及分析应用。L-Alanine is a non-essential amino acid, involved in sugar and acid metabolism, increases immunity, and provides energy for muscle tissue, brain, and central nervous system.
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.
