布雷非德菌素 A
Brefeldin A (BFA) 是一种内酯抗生素，是蛋白质运输的特定抑制剂。Brefeldin A 阻断分泌蛋白和膜蛋白从内质网向高尔基体的转运。Brefeldin A 也是一种自噬 (autophagy) 和 mitophagy 抑制剂。Brefeldin A 可抑制 HSV-1病毒，并具有抗癌活性。
Soyasaponin II 是具有抗病毒活性的皂苷。Soyasaponin II 抑制 HSV-1，HCMV，流感病毒和 HIV-1 的复制。Soyasaponin II 对 HSV-1 复制显示出有效的抑制作用。Soyasaponin II 作为 YB-1 磷酸化和 NLRP3 炎性小体引发的抑制剂，可保护小鼠免受 LPS/GalN 诱导的急性肝衰竭。
布雷非德菌素 A (标准品)
Brefeldin A (Standard) (BFA (Standard)) 是 Brefeldin A 的分析标准品。本产品用于研究及分析应用。Brefeldin A (BFA) 是一种内酯抗生素，是蛋白质运输的特定抑制剂。Brefeldin A 阻断分泌蛋白和膜蛋白从内质网向高尔基体的转运。Brefeldin A 也是一种自噬 (autophagy) 和 mitophagy 抑制剂。Brefeldin A 可抑制 HSV-1病毒，并具有抗癌活性。
Verlamelin A 是一种具有抗真菌 (fungal) 和抗病毒活性的大环缩肽。Verlamelin A 对花斑曲霉和澳大利亚弯孢霉显示出抗真菌活性，并且对 HSV-1 也具有抗病毒活性 (IC50 = 16.7 μM)。Verlamelin A 可以从昆虫病原真菌 Lecanicillium sp. 分离。Verlamelin A 可用于抗真菌和抗病毒研究。
大豆甾醇A (标准品)
Soyasapogenol A (Standard) 是 Soyasapogenol A (HY-N6073) 的分析标准品。本产品用于研究及分析应用。Soyasapogenol A 是大豆皂苷的三萜类苷元。Soyasapogenol A 具有抗炎、抗癌、保肝和抗HSV-1 等活性。Soyasapogenol A 可用于肿瘤和免疫炎症性疾病的研究。
Defensin HNP-1 human 是一种人中性粒细胞肽 (HNPs)。Defensin HNP-1 human 具有免疫调节功能，可延迟中性粒细胞凋亡 (apoptosis)。Defensin HNP-1 human 通过抑制 DNA/RNA/蛋白质合成，干扰代谢途径，具有广泛的抗菌活性。Defensin HNP-1 human 对 HIV、HSV-1、HSV-2、CMV、流感病毒等有直接灭活作用。Defensin HNP-1 human 具有抗利什曼原虫活性。Defensin HNP-1 human 参与早期动脉粥样硬化发展时的内皮细胞功能障碍。
Defensin HNP-1 human TFA 是一种人中性粒细胞肽 (HNPs)。Defensin HNP-1 human TFA 具有免疫调节功能，可延迟中性粒细胞凋亡 (apoptosis)。Defensin HNP-1 human TFA 通过抑制 DNA/RNA/蛋白质合成，干扰代谢途径，具有广泛的抗菌活性。Defensin HNP-1 human TFA 对 HIV、HSV-1、HSV-2、CMV、流感病毒等有直接灭活作用。Defensin HNP-1 human TFA 具有抗利什曼原虫活性。Defensin HNP-1 human TFA 参与早期动脉粥样硬化发展时的内皮细胞功能障碍。
Peniterphenyl A 是一种从深海衍生的青霉属植物中获得的天然产物。Peniterphenyl A 抑制 HSV-1/2 病毒进入细胞，并可能通过与病毒包膜糖蛋白 D 直接相互作用来干扰病毒吸附和膜融合，从而阻断 HSV-1/2 感染。Peniterphenyl A 是一种很有前途的抗 HSV-1/2 的先导化合物。
3-Deaza-2’-deoxyadenosine 是由 2’-脱氧腺苷合成的核苷类似物。3-Deaza-2’-deoxyadenosine 通过与核糖核苷酸的核糖片段结合来抑制 RNA 合成，从而阻止酶-底物复合物的形成，从而阻止链的延伸，也能够通过结合 DNA 的脱氧核糖片段和阻止 DNA 聚合酶向生长链添加核苷酸来抑制 DNA 合成。3-Deaza-2’-deoxyadenosine 具有抗病毒 (antiviral) 活性。
Defensin HNP-1 human 是一种人中性粒细胞肽 (HNPs)。Defensin HNP-1 human 具有免疫调节功能，可延迟中性粒细胞凋亡 (apoptosis)。Defensin HNP-1 human 通过抑制 DNA/RNA/蛋白质合成，干扰代谢途径，具有广泛的抗菌活性。Defensin HNP-1 human 对 HIV、HSV-1、HSV-2、CMV、流感病毒等有直接灭活作用。Defensin HNP-1 human 具有抗利什曼原虫活性。Defensin HNP-1 human 参与早期动脉粥样硬化发展时的内皮细胞功能障碍。
Defensin HNP-1 human TFA 是一种人中性粒细胞肽 (HNPs)。Defensin HNP-1 human TFA 具有免疫调节功能，可延迟中性粒细胞凋亡 (apoptosis)。Defensin HNP-1 human TFA 通过抑制 DNA/RNA/蛋白质合成，干扰代谢途径，具有广泛的抗菌活性。Defensin HNP-1 human TFA 对 HIV、HSV-1、HSV-2、CMV、流感病毒等有直接灭活作用。Defensin HNP-1 human TFA 具有抗利什曼原虫活性。Defensin HNP-1 human TFA 参与早期动脉粥样硬化发展时的内皮细胞功能障碍。
Verlamelin A 是一种具有抗真菌 (fungal) 和抗病毒活性的大环缩肽。Verlamelin A 对花斑曲霉和澳大利亚弯孢霉显示出抗真菌活性，并且对 HSV-1 也具有抗病毒活性 (IC50 = 16.7 μM)。Verlamelin A 可以从昆虫病原真菌 Lecanicillium sp. 分离。Verlamelin A 可用于抗真菌和抗病毒研究。
布雷非德菌素 A
Brefeldin A (BFA) 是一种内酯抗生素，是蛋白质运输的特定抑制剂。Brefeldin A 阻断分泌蛋白和膜蛋白从内质网向高尔基体的转运。Brefeldin A 也是一种自噬 (autophagy) 和 mitophagy 抑制剂。Brefeldin A 可抑制 HSV-1病毒，并具有抗癌活性。
Soyasaponin II 是具有抗病毒活性的皂苷。Soyasaponin II 抑制 HSV-1，HCMV，流感病毒和 HIV-1 的复制。Soyasaponin II 对 HSV-1 复制显示出有效的抑制作用。Soyasaponin II 作为 YB-1 磷酸化和 NLRP3 炎性小体引发的抑制剂，可保护小鼠免受 LPS/GalN 诱导的急性肝衰竭。
布雷非德菌素 A (标准品)
Brefeldin A (Standard) (BFA (Standard)) 是 Brefeldin A 的分析标准品。本产品用于研究及分析应用。Brefeldin A (BFA) 是一种内酯抗生素，是蛋白质运输的特定抑制剂。Brefeldin A 阻断分泌蛋白和膜蛋白从内质网向高尔基体的转运。Brefeldin A 也是一种自噬 (autophagy) 和 mitophagy 抑制剂。Brefeldin A 可抑制 HSV-1病毒，并具有抗癌活性。
Verlamelin A 是一种具有抗真菌 (fungal) 和抗病毒活性的大环缩肽。Verlamelin A 对花斑曲霉和澳大利亚弯孢霉显示出抗真菌活性，并且对 HSV-1 也具有抗病毒活性 (IC50 = 16.7 μM)。Verlamelin A 可以从昆虫病原真菌 Lecanicillium sp. 分离。Verlamelin A 可用于抗真菌和抗病毒研究。
大豆甾醇A (标准品)
Soyasapogenol A (Standard) 是 Soyasapogenol A (HY-N6073) 的分析标准品。本产品用于研究及分析应用。Soyasapogenol A 是大豆皂苷的三萜类苷元。Soyasapogenol A 具有抗炎、抗癌、保肝和抗HSV-1 等活性。Soyasapogenol A 可用于肿瘤和免疫炎症性疾病的研究。
Peniterphenyl A 是一种从深海衍生的青霉属植物中获得的天然产物。Peniterphenyl A 抑制 HSV-1/2 病毒进入细胞，并可能通过与病毒包膜糖蛋白 D 直接相互作用来干扰病毒吸附和膜融合，从而阻断 HSV-1/2 感染。Peniterphenyl A 是一种很有前途的抗 HSV-1/2 的先导化合物。
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.
