核糖核酸酶A
RNase A (Bovine pancreatic RNase) 是一种广泛用于 DNA 纯化的核酸内切酶 (Endonuclease)，它能特异性水解 RNA 中的胞嘧啶或尿嘧啶残基。RNase A 可降解 RNA/DNA 双链体中的 RNA。RNase A 催化单链 RNA 的 3',5'-磷酸二酯键断裂。生物体内的 RNase A 家族成员与多种生理和病理过程密切相关，包括细胞生长发育、增殖、分化和迁移。RNase A 活性或表达水平的失调与胰腺癌、卵巢癌、膀胱癌和甲状腺癌密切相关。RNase A 具有杀伤肿瘤细胞的能力。
重组核糖核酸酶A (无动物源)
RNase A (Bovine pancreatic RNase) 是一种广泛用于 DNA 纯化的核酸内切酶 (Endonuclease)，它能特异性水解 RNA 中的胞嘧啶或尿嘧啶残基。RNase A 可降解 RNA/DNA 双链体中的 RNA。RNase A 催化单链 RNA 的 3',5'-磷酸二酯键断裂。生物体内的 RNase A 家族成员与多种生理和病理过程密切相关，包括细胞生长发育、增殖、分化和迁移。RNase A 活性或表达水平的失调与胰腺癌、卵巢癌、膀胱癌和甲状腺癌密切相关。RNase A 具有杀伤肿瘤细胞的能力。RNase A, Recombinant (animal free) 是重组 RNase A，无动物源性成分。
核糖核酸酶 A, 重组
RNase A (Bovine pancreatic RNase) 是一种广泛用于 DNA 纯化的核酸内切酶 (Endonuclease)，它能特异性水解 RNA 中的胞嘧啶或尿嘧啶残基。RNase A 可降解 RNA/DNA 双链体中的 RNA。RNase A 催化单链 RNA 的 3',5'-磷酸二酯键断裂。生物体内的 RNase A 家族成员与多种生理和病理过程密切相关，包括细胞生长发育、增殖、分化和迁移。RNase A 活性或表达水平的失调与胰腺癌、卵巢癌、膀胱癌和甲状腺癌密切相关。RNase A 具有杀伤肿瘤细胞的能力。RNase A, Recombinant (Ribonuclease A, Recombinant) 是重组的 RNase A。
核糖核酸酶 A (不含 DNase 和蛋白酶), 重组
RNase A (Bovine pancreatic RNase) 是一种广泛用于 DNA 纯化的核酸内切酶 (Endonuclease)，它能特异性水解 RNA 中的胞嘧啶或尿嘧啶残基。RNase A 可降解 RNA/DNA 双链体中的 RNA。RNase A 催化单链 RNA 的 3',5'-磷酸二酯键断裂。生物体内的 RNase A 家族成员与多种生理和病理过程密切相关，包括细胞生长发育、增殖、分化和迁移。RNase A 活性或表达水平的失调与胰腺癌、卵巢癌、膀胱癌和甲状腺癌密切相关。RNase A 具有杀伤肿瘤细胞的能力。RNase A (DNase & Protease Free), Recombinant 是重组的 RNase A，不含 DNase 和蛋白酶。
RNase A (Bovine pancreatic RNase) 是一种广泛用于 DNA 纯化的核酸内切酶 (Endonuclease)，它能特异性水解 RNA 中的胞嘧啶或尿嘧啶残基。RNase A 可降解 RNA/DNA 双链体中的 RNA。RNase A 催化单链 RNA 的 3',5'-磷酸二酯键断裂。生物体内的 RNase A 家族成员与多种生理和病理过程密切相关，包括细胞生长发育、增殖、分化和迁移。RNase A 活性或表达水平的失调与胰腺癌、卵巢癌、膀胱癌和甲状腺癌密切相关。RNase A 具有杀伤肿瘤细胞的能力。RNase A, Bovine Pancreas (DNase & Protease Free) 是牛胰腺来源 RNase A，不含 DNase 和蛋白酶。
TANDEM (Des-N-tetramethyltriostin A)是一种合成的抗生素类药物，具有抑制肿瘤细胞生长的活性。TANDEM可用于联合化疗以增强抑制效果。TANDEM在体外实验中显示出对多种癌细胞系的显著抑制作用。TANDEM的结构使其在抑制过程中可以有效地靶向肿瘤细胞。TANDEM的作用机制涉及干扰细胞增殖与存活途径。
神经肽是神经元通过调节分泌途径产生和释放的小蛋白物质，在神经元中表达并具有递质或共递质功能，并作用于神经底物。神经肽是迄今为止大脑中最大和最多样化的信号分子，与疾病的发生和药物的开发息息相关。神经肽参与到炎症和免疫类疾病的发生，并对上皮细胞、血管细胞和结缔组织细胞的增殖和组织修复产生影响。已有研究表明，神经肽在神经系统受到挑战（如压力、损伤或滥用药物）时具有特别重要的作用。Substance P 是一种神经肽，在中枢神经系统中作为神经递质和神经调节剂，目前处于临床研究阶段，被证明与炎症过程和疼痛有关。
TANDEM (Des-N-tetramethyltriostin A)是一种合成的抗生素类药物，具有抑制肿瘤细胞生长的活性。TANDEM可用于联合化疗以增强抑制效果。TANDEM在体外实验中显示出对多种癌细胞系的显著抑制作用。TANDEM的结构使其在抑制过程中可以有效地靶向肿瘤细胞。TANDEM的作用机制涉及干扰细胞增殖与存活途径。
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.
