Protein A (SPA) 是一种存在于细菌表面并可自由分泌到细胞外环境中的免疫球蛋白 (Ig) 结合蛋白。Protein A 通过结合抗体的 Fc 区和 B 细胞受体的 Fab 区，从而阻断调理吞噬作用并在体外导致 B 细胞凋亡 (apoptosis)。Protein A 可与 IgG 形成毒性免疫复合物，进而诱导白细胞坏死。Protein A 有助于金黄色葡萄球菌的毒力表达。Protein A 在经 IgG 预处理的小鼠模型中引发过敏反应。Protein A 可用于免疫系统疾病的相关的研究。
人免疫球蛋白M
Human Immunoglobulin M (IgM) 是适应性免疫系统对外来抗原产生的应答而分泌的抗体。Human Immunoglobulin M 是一类主要的免疫球蛋白，在原发性抗体反应的早期阶段分泌到血液循环中。Human Immunoglobulin M 是由 5 个 IgG 当量组成的五聚体，包含 10 个 Fab 片段，因此有 10 个抗原结合位点。Human Immunoglobulin M 是一种补体 (complement) 激活剂。
Human secretory immunoglobulin A 是大多数黏膜表面的主要免疫球蛋白。Human secretory immunoglobulin A 是一种多肽复合物，由两个 IgA 单体、一条连接 J 链和分泌成分组成。Human secretory immunoglobulin A 位于黏膜表面，通过阻止病原体入侵来提供保护。
弹性蛋白酶来源于人类白血球
Elastase, Human leukocytes 是一种丝氨酸蛋白酶，存在于中性粒细胞的亲氮颗粒中。Elastase, Human leukocytes 潜在底物包括细胞外基质的几乎所有成分，以及凝血因子、补体、免疫球蛋白和细胞因子等多种蛋白质，有强大的蛋白质水解功能，参与炎症组织损伤的发病机制。
Efdelikofusp alfa 是一种双特异性 Fc 融合蛋白，由人 CD80 (B7.1) 的 N 端胞外结构域与人免疫球蛋白G4 (IgG4) Fc 片段融合，并作为 C 端部分与白细胞介素-2 变体 (IL-2v) 连接。Efdelikofusp alfa 具有潜在的免疫刺激、免疫检查点抑制和抗肿瘤活性。
Efzilonkofusp alfa 是一种双特异性 Fc 融合蛋白，由人 CD80 (B7.1) 的 N 端胞外结构域与人免疫球蛋白G4 (IgG4) Fc 片段融合，并作为 C 端部分与白细胞介素-2 变体 (IL-2v) 连接。Efzilonkofusp alfa 具有潜在的免疫刺激、免疫检查点抑制和抗肿瘤活性。
Protein A (SPA) 是一种存在于细菌表面并可自由分泌到细胞外环境中的免疫球蛋白 (Ig) 结合蛋白。Protein A 通过结合抗体的 Fc 区和 B 细胞受体的 Fab 区，从而阻断调理吞噬作用并在体外导致 B 细胞凋亡 (apoptosis)。Protein A 可与 IgG 形成毒性免疫复合物，进而诱导白细胞坏死。Protein A 有助于金黄色葡萄球菌的毒力表达。Protein A 在经 IgG 预处理的小鼠模型中引发过敏反应。Protein A 可用于免疫系统疾病的相关的研究。
人免疫球蛋白M
Human Immunoglobulin M (IgM) 是适应性免疫系统对外来抗原产生的应答而分泌的抗体。Human Immunoglobulin M 是一类主要的免疫球蛋白，在原发性抗体反应的早期阶段分泌到血液循环中。Human Immunoglobulin M 是由 5 个 IgG 当量组成的五聚体，包含 10 个 Fab 片段，因此有 10 个抗原结合位点。Human Immunoglobulin M 是一种补体 (complement) 激活剂。
Human secretory immunoglobulin A 是大多数黏膜表面的主要免疫球蛋白。Human secretory immunoglobulin A 是一种多肽复合物，由两个 IgA 单体、一条连接 J 链和分泌成分组成。Human secretory immunoglobulin A 位于黏膜表面，通过阻止病原体入侵来提供保护。
Efdelikofusp alfa 是一种双特异性 Fc 融合蛋白，由人 CD80 (B7.1) 的 N 端胞外结构域与人免疫球蛋白G4 (IgG4) Fc 片段融合，并作为 C 端部分与白细胞介素-2 变体 (IL-2v) 连接。Efdelikofusp alfa 具有潜在的免疫刺激、免疫检查点抑制和抗肿瘤活性。
Efzilonkofusp alfa 是一种双特异性 Fc 融合蛋白，由人 CD80 (B7.1) 的 N 端胞外结构域与人免疫球蛋白G4 (IgG4) Fc 片段融合，并作为 C 端部分与白细胞介素-2 变体 (IL-2v) 连接。Efzilonkofusp alfa 具有潜在的免疫刺激、免疫检查点抑制和抗肿瘤活性。
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.
