地骨皮甲素
Kukoamine A 是一种具有口服活性可穿透血脑屏障的精胺类生物碱，被发现存在于宁夏枸杞 (Lycium chinense，L. chinense) Miller 的根皮中。Kukoamine A 可抑制纯化的簇生锥虫锥虫硫醇还原酶和大豆脂氧合酶 (lipoxygenase)，并激活 μ-阿片 (μ-opioid) 受体。Kukoamine A 能够抑制癌细胞增殖、迁移和侵袭，引起 G0/G1 期细胞周期阻滞并诱导细胞凋亡 (apoptosis)。Kukoamine A 具有神经保护作用，还可诱导自噬 (autophagy)。Kukoamine A 可抑制 LPS (HY-D1056) 诱导的 NO、ROS、PGE2、TNF-α、IL-1β、IL-6 的产生以及 COX-2 的活性。Kukoamine A 可通过下调 Srebp-1c 逆转棕榈酸诱导胰岛素抵抗、脂质蓄积和氧化应激。Kukoamine A 可用于癌症、感染、炎症、代谢性疾病和神经系统疾病的研究，例如胶质母细胞瘤和帕金森病。
Biocytin-β-endorphin, human 是一种生物素标记的 β-Endorphin, human (HY-P1502)。β-Endorphin, human 是存在于垂体和下丘脑中的重要的内源性肽，为阿片样 (opioid) 受体激动剂，尤其对 μ-opioid 受体和 δ-opioid 受体的亲和性更高；β-Endorphin, human 具有缓解疼痛的功效。
BPRMU191 是一种 μ-阿片受体 (MOR) 调节剂，通过将小分子吗啡类拮抗剂转变为 G 蛋白偏向的 MOR 激动剂，诱导 MOR 激活，从而发挥镇痛作用。BPRMU191 与吗啡类拮抗剂联合使用，可在减少副作用的同时提供 MOR-依赖性镇痛效果，显著降低了胃肠功能障碍、抗伤害性感受耐受性以及依赖性不良反应。BPRMU191 与吗啡类拮抗剂的联合应用可作为研究重度疼痛的潜在策略，同时为研究 G 蛋白偶联受体调节提供了新思路。
Biocytin-β-endorphin, human 是一种生物素标记的 β-Endorphin, human (HY-P1502)。β-Endorphin, human 是存在于垂体和下丘脑中的重要的内源性肽，为阿片样 (opioid) 受体激动剂，尤其对 μ-opioid 受体和 δ-opioid 受体的亲和性更高；β-Endorphin, human 具有缓解疼痛的功效。
地骨皮甲素
Kukoamine A 是一种具有口服活性可穿透血脑屏障的精胺类生物碱，被发现存在于宁夏枸杞 (Lycium chinense，L. chinense) Miller 的根皮中。Kukoamine A 可抑制纯化的簇生锥虫锥虫硫醇还原酶和大豆脂氧合酶 (lipoxygenase)，并激活 μ-阿片 (μ-opioid) 受体。Kukoamine A 能够抑制癌细胞增殖、迁移和侵袭，引起 G0/G1 期细胞周期阻滞并诱导细胞凋亡 (apoptosis)。Kukoamine A 具有神经保护作用，还可诱导自噬 (autophagy)。Kukoamine A 可抑制 LPS (HY-D1056) 诱导的 NO、ROS、PGE2、TNF-α、IL-1β、IL-6 的产生以及 COX-2 的活性。Kukoamine A 可通过下调 Srebp-1c 逆转棕榈酸诱导胰岛素抵抗、脂质蓄积和氧化应激。Kukoamine A 可用于癌症、感染、炎症、代谢性疾病和神经系统疾病的研究，例如胶质母细胞瘤和帕金森病。
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.
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