Anti-CD68 antibody [C68/684] (Ab201340)
CD68, Macrosialin, Gp110
用户验证的应用
推荐稀释比例
- IHC-P1-2 µg/mL Perform heat mediated antigen retrieval with 10 mM Tris with 1 mM EDTA buffer pH 9.0 for 45 minutes at 95°C followed by cooling at RT for 20 minutes. Incubate with primary for 30 minutes at RT.
- WB1-2 µg/mL
- ICC/IF1-2 µg/mL
- Flow Cyt1-2 µg for 10^6 Cells ab170190 - Mouse monoclonal IgG1, is suitable for use as an isotype control with this antibody.
详细信息
背景信息
Anti-CD68 antibody [C68/684] (ab201340) is a House Mouse Monoclonal antibody and is validated for use in Flow Cyt, ICC/IF, IHC-P, WB in human samples. Anti-CD68 antibody [C68/684] (ab201340) has been cited over 105 times in peer reviewed journals and is trusted by the scientific community. Abcams high quality validation processes ensure Anti-CD68 antibody [C68/684] (ab201340) has high sensitivity and specificity. Anti-CD68 antibody [C68/684] (ab201340) specifically detects CD68 (UniProt ID: P34810; Molecular weight: 35kDa) and is sold in 100 uL selling sizes. Conjugation-ready, carrier free format available for antibody clone C68/684 - ab21398. CD68 is a marker primarily associated with macrophages, playing a crucial role in phagocytosis, antigen presentation, and immune response regulation. CD68 is a biomarker in chronic inflammatory conditions including rheumatoid arthritis and inflammatory bowel disease ab201340 stains macrophages in a wide variety of Human tissues, including Kupffer cells and macrophages in the red pulp of the spleen, in lamina propria of the gut, in lung alveoli, and in bone marrow. It reacts with myeloid precursors and peripheral blood granulocytes. It also reacts with plasmacytoid T cells, which are supposed to be of monocyte/macrophage origin. It shows strong granular cytoplasmic staining of chronic and acute myeloid leukemia and also reacts with rare cases of true histiocytic neoplasia. Lymphomas are negative or show few granules.
文献引用 (149)
Airway immune profiles and therapeutic implications of IGF1 in eosinophilic granulomatosis with polyangiitis.
嗜酸性肉芽肿性血管炎中 IGF1 的气道免疫特征和治疗意义。
Pharmacological Microglial Inhibition Remodels the Scar Microenvironment to Support Reticulospinal Circuit Reconstruction After Spinal Cord Injury.
药物抑制小胶质细胞可重塑瘢痕微环境,从而支持脊髓损伤后网状脊髓回路的重建。
CEBPB-high dormant tumor cells drive immune evasion via S100A8 orchestrated tumor-associated macrophages reprogramming
CEBPB高表达的休眠肿瘤细胞通过S100A8调控的肿瘤相关巨噬细胞重编程驱动免疫逃逸
Proteogenomic characterization delineates clinically relevant subtypes of advanced differentiated thyroid cancer.
蛋白质基因组学特征分析可以区分具有临床意义的晚期分化型甲状腺癌亚型。
In the diffuse large B-cell lymphoma microenvironment, SIRT1 is upregulated and correlated with a pro-inflammatory macrophage signature and autophagy-related gene expression.
在弥漫性大B细胞淋巴瘤微环境中,SIRT1 上调,并与促炎巨噬细胞特征和自噬相关基因表达相关。
Nocardia rubra cell wall skeleton-induced MARCO expression: implications for improved phagocytosis and cytokine secretion in tumor-associated macrophages.
诺卡氏菌细胞壁骨架诱导的 MARCO 表达:对肿瘤相关巨噬细胞吞噬作用和细胞因子分泌的改善具有重要意义。
650 nm red-light therapy attenuates sepsis-induced acute lung injury via adiponectin-mediated immune-metabolic reprogramming.
650纳米红光疗法通过脂联素介导的免疫代谢重编程减轻脓毒症引起的急性肺损伤。
Porcine decellularized nerve matrix hydrogel attenuates neuroinflammation after peripheral nerve injury by inhibiting the TLR4/MyD88/NF-κB axis
猪源脱细胞神经基质水凝胶通过抑制TLR4/MyD88/NF-κB轴减轻周围神经损伤后的神经炎症。
TWEAK modulates the characteristics of periodontal ligament stem cells via the Fn14/NFâκB pathway.
TWEAK 通过 Fn14/NF-αB 通路调节牙周膜干细胞的特性。
Static Magnetic Field-Mediated Parathyroid Xenotransplantation Modulates Lymphocyte Migration: A Potential Immunosuppression-Free Long-Term Treatment for Hypoparathyroidism.
静态磁场介导的甲状旁腺异种移植调节淋巴细胞迁移:一种潜在的无需免疫抑制的甲状旁腺功能减退症长期治疗方法。
- 1
- 2
- 3
- 4
- 5
- 6
- 15