Bisindolylmaleimide X hydrochloride (Ro 31-8425 hydrochloride, BIM-X hydrochloride) 是一种可渗透细胞的蛋白激酶 C (PKC) 抑制剂。Bisindolylmaleimide X hydrochloride 也是一种有效的细胞周期蛋白依赖性激酶 2 (CDK2) 拮抗剂，IC50 为 200 nM。Bisindolylmaleimide X hydrochloride 抑制体外 CD4 T 细胞的增殖。Bisindolylmaleimide X hydrochloride 抑制人胚静脉内皮细胞的 eNOS-Ser1177 磷酸化。Bisindolylmaleimide X hydrochloride 可用于免疫系统和心脑血管疾病的研究。
L-Guluronic acid sodium salt 是一种凝血因子 Xa (coagulation factor X) 抑制剂。L-Guluronic acid sodium salt 可替代类肝素抗凝五糖中的 L-Iduronic acid (HY-135197)，同时保留凝血因子 Xa 抑制活性。L-Guluronic acid sodium salt 可用于深静脉血栓、肺栓塞等凝血障碍疾病的研究。
[D-Pro2,D-Phe7,D-Trp9] Substance P 是 Substance P (HY-P0201) 的类似物。[D-Pro2,D-Phe7,D-Trp9] Substance P 是 Substance P 的抑制剂。[D-Pro2,D-Phe7,D-Trp9] Substance P 间接收缩豚鼠回肠。
Bisindolylmaleimide X (Ro 31-8425, BIM-X) 是一种可渗透细胞的蛋白激酶 C (PKC) 抑制剂。Bisindolylmaleimide X 也是一种有效的细胞周期蛋白依赖性激酶 2 (CDK2) 拮抗剂，IC50 为 200 nM。Bisindolylmaleimide X 抑制体外 CD4 T 细胞的增殖。Bisindolylmaleimide X 抑制人胚静脉内皮细胞的 eNOS-Ser1177 磷酸化。Bisindolylmaleimide X 可用于免疫系统和心脑血管疾病的研究。
Dammarenediol II 是一种人参皂苷前体。Dammarenediol II 降低 O-GlcNAc 转移酶 (OGT) 活性并下调整体 O-乙酰氨基葡萄糖化水平。Dammarenediol II 可抑制 Akt、mTOR 和 GSK3β 的磷酸化。Dammarenediol II 可抑制人源羧酸酯酶活性、VEGF 诱导的 ROS 生成、应力纤维形成以及血管内皮钙粘蛋白的破坏。Dammarenediol II 可促进细胞凋亡 (apoptosis)，提高剪切型 PARP1 和 p53 的水平，并抑制视网膜微血管渗漏。Dammarenediol II 可用于肝癌、糖尿病视网膜病变相关研究。
麦冬皂苷D
Ophiopogonin D 是可以从麦冬 (Ophiopogon japonicus) 的块茎中分离的，是一种罕见的天然存在的 C29 甾体糖苷。Ophiopogonin D 是 CYP2J3 诱导剂，其通过增加人脐静脉内皮细胞 (HUVECs) 中 CYP2J2/EETs 和 PPARα 的表达，显着抑制 Ang II 诱导的 NF-κB 核转位，IκBα 下调，细胞内 Ca2+ 过载和促炎细胞因子的激活。Ophiopogonin D 能抑制 RAW264.7 细胞的破骨细胞分化。Ophiopogonin D 作为抗氧化剂，在过氧化氢 (H2O2) 诱导的内皮损伤中具有保护作用。Ophiopogonin D 能阻断 ERK 信号级联。Ophiopogonin D 可缓解高脂饮食引起的代谢综合征，并改变小鼠肠道菌群的结构。Ophiopogonin D 已被用于炎症、代谢和心血管疾病。
麦冬皂苷D (标准品)
Ophiopogonin D (Standard) 是 Ophiopogonin D 的分析标准品。本产品用于研究及分析应用。Ophiopogonin D 是可以从麦冬 (Ophiopogon japonicus) 的块茎中分离的，是一种罕见的天然存在的 C29 甾体糖苷。Ophiopogonin D 是 CYP2J3 诱导剂，其通过增加人脐静脉内皮细胞 (HUVECs) 中 CYP2J2/EETs 和 PPARα 的表达，显着抑制 Ang II 诱导的 NF-κB 核转位，IκBα 下调，细胞内 Ca2+ 过载和促炎细胞因子的激活。Ophiopogonin D 能抑制 RAW264.7 细胞的破骨细胞分化。Ophiopogonin D 作为抗氧化剂，在过氧化氢 (H2O2) 诱导的内皮损伤中具有保护作用。Ophiopogonin D 能阻断 ERK 信号级联。Ophiopogonin D 可缓解高脂饮食引起的代谢综合征，并改变小鼠肠道菌群的结构。Ophiopogonin D 已被用于炎症、代谢和心血管疾病。
Striatisporolide A 是一种抗菌剂。Striatisporolide A 在体外对 Escherichia coli 具有抑菌活性。Striatisporolide A 会损伤 Escherichia coli 的细胞壁与细胞膜，诱导蛋白水平及形态学改变。Striatisporolide A 降低 HUVECs 凋亡 (apoptosis) 水平，并抑制 ROS 过量产生，具有促细胞增殖作用及轻微的细胞保护作用。Striatisporolide A 可用于细菌 (bacterial) 感染及退行性疾病的相关研究。
乙酸钾,用于分子生物学
Potassium acetate, for molecular biology 是一种乙酸盐，常用作除冰剂、食品防腐剂和钾源。Potassium acetate 可升高乙酰辅酶 A 水平。Potassium acetate, for molecular biology 可作为制备废茶基活性炭的活化剂，用于 Acid Blue 25染料的吸附。
乙酸钾,用于分子生物学
Potassium acetate, for molecular biology 是一种乙酸盐，常用作除冰剂、食品防腐剂和钾源。Potassium acetate 可升高乙酰辅酶 A 水平。Potassium acetate, for molecular biology 可作为制备废茶基活性炭的活化剂，用于 Acid Blue 25染料的吸附。
[D-Pro2,D-Phe7,D-Trp9] Substance P 是 Substance P (HY-P0201) 的类似物。[D-Pro2,D-Phe7,D-Trp9] Substance P 是 Substance P 的抑制剂。[D-Pro2,D-Phe7,D-Trp9] Substance P 间接收缩豚鼠回肠。
麦冬皂苷D
Ophiopogonin D 是可以从麦冬 (Ophiopogon japonicus) 的块茎中分离的，是一种罕见的天然存在的 C29 甾体糖苷。Ophiopogonin D 是 CYP2J3 诱导剂，其通过增加人脐静脉内皮细胞 (HUVECs) 中 CYP2J2/EETs 和 PPARα 的表达，显着抑制 Ang II 诱导的 NF-κB 核转位，IκBα 下调，细胞内 Ca2+ 过载和促炎细胞因子的激活。Ophiopogonin D 能抑制 RAW264.7 细胞的破骨细胞分化。Ophiopogonin D 作为抗氧化剂，在过氧化氢 (H2O2) 诱导的内皮损伤中具有保护作用。Ophiopogonin D 能阻断 ERK 信号级联。Ophiopogonin D 可缓解高脂饮食引起的代谢综合征，并改变小鼠肠道菌群的结构。Ophiopogonin D 已被用于炎症、代谢和心血管疾病。
Dammarenediol II 是一种人参皂苷前体。Dammarenediol II 降低 O-GlcNAc 转移酶 (OGT) 活性并下调整体 O-乙酰氨基葡萄糖化水平。Dammarenediol II 可抑制 Akt、mTOR 和 GSK3β 的磷酸化。Dammarenediol II 可抑制人源羧酸酯酶活性、VEGF 诱导的 ROS 生成、应力纤维形成以及血管内皮钙粘蛋白的破坏。Dammarenediol II 可促进细胞凋亡 (apoptosis)，提高剪切型 PARP1 和 p53 的水平，并抑制视网膜微血管渗漏。Dammarenediol II 可用于肝癌、糖尿病视网膜病变相关研究。
麦冬皂苷D (标准品)
Ophiopogonin D (Standard) 是 Ophiopogonin D 的分析标准品。本产品用于研究及分析应用。Ophiopogonin D 是可以从麦冬 (Ophiopogon japonicus) 的块茎中分离的，是一种罕见的天然存在的 C29 甾体糖苷。Ophiopogonin D 是 CYP2J3 诱导剂，其通过增加人脐静脉内皮细胞 (HUVECs) 中 CYP2J2/EETs 和 PPARα 的表达，显着抑制 Ang II 诱导的 NF-κB 核转位，IκBα 下调，细胞内 Ca2+ 过载和促炎细胞因子的激活。Ophiopogonin D 能抑制 RAW264.7 细胞的破骨细胞分化。Ophiopogonin D 作为抗氧化剂，在过氧化氢 (H2O2) 诱导的内皮损伤中具有保护作用。Ophiopogonin D 能阻断 ERK 信号级联。Ophiopogonin D 可缓解高脂饮食引起的代谢综合征，并改变小鼠肠道菌群的结构。Ophiopogonin D 已被用于炎症、代谢和心血管疾病。
Striatisporolide A 是一种抗菌剂。Striatisporolide A 在体外对 Escherichia coli 具有抑菌活性。Striatisporolide A 会损伤 Escherichia coli 的细胞壁与细胞膜，诱导蛋白水平及形态学改变。Striatisporolide A 降低 HUVECs 凋亡 (apoptosis) 水平，并抑制 ROS 过量产生，具有促细胞增殖作用及轻微的细胞保护作用。Striatisporolide A 可用于细菌 (bacterial) 感染及退行性疾病的相关研究。
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.
![[Pro34]Neuropeptide Y, porcine](http://hg.y866.cn/biomolecule/lib/file/product_pic/hy-p10291.gif)
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