Anti-Histone H3 (citrulline R2 + R8 + R17) antibody (Ab5103)
H3FA, HIST1H3A, H3C2, H3FL, HIST1H3B, H3C3, H3FC HIST1H3C, H3C4, H3FB, HIST1H3D, H3C6, H3FD, HIST1H3E, H3C7, H3FI, HIST1H3F, H3C8, H3FH, HIST1H3G, H3C10, H3FK, HIST1H3H, H3C11, H3FF, HIST1H3I, H3C12, H3FJ, HIST1H3J, H3C1, H3FC, HIST1H3C, Histone H3.1, Histone H3/a, Histone H3/b, Histone H3/c, Histone H3/d, Histone H3/f, Histone H3/h, Histone H3/i, Histone H3/j, Histone H3/k, Histone H3/l, H3R2cit
详细信息
特异性
In peptide array this product recognises the Histone H3 (citrulline R2+R8+R17) peptide and shows minimal crossreactivity with the nonmodified peptide. Treatment is required for detection of the target protein. See Protocol section for detailed information. 更多详细信息请参阅 Protocol 部分.
背景信息
Anti-Histone H3 (citrulline R2 + R8 + R17) antibody (ab5103) is a rabbit polyclonal antibody and is validated for use in IP, PepArr and WB. Anti-Histone H3 (citrulline R2 + R8 + R17) antibody (ab5103) was first used in a scientific publication in 2004 and has been cited over 595 times in peer reviewed journals. Abcam's high quality validation processes ensure Anti-Histone H3 (citrulline R2 + R8 + R17) antibody (ab5103) has high sensitivity and specificity. Anti-Histone H3 (citrulline R2 + R8 + R17) antibody (ab5103) has 27 independent reviews from customers. Anti-Histone H3 (citrulline R2 + R8 + R17) antibody (ab5103) specifically detects Histone H3 Citrulline-R2, Citrulline-R8, Citrulline-R17 (UniProt ID: P68431; Molecular weight: 16kDa) and is sold in 100 µg selling sizes. Top cited antibody for this target with >800 citations. This antibody is a key tool in cancer research, particularly in understanding histone citrullination's role in tumorigenesis and is widely used in studies of gene expression, DNA repair and autoimmune diseases like rheumatoid arthritis and lupus, involving protein arginine deiminases (PADs) and NETosis. Histone hypercitrullination is reported to play a role the progression of various cancers, including multiple myeloma, acute myeloid leukaemia, lung cancer and hepatocellular carcinoma.
文献引用 (836)
IL-36γ armored CAR T cells reprogram neutrophils to induce endogenous antitumor immunity.
IL-36α 装甲 CAR T 细胞可重编程中性粒细胞,诱导内源性抗肿瘤免疫。
The Ly6g(high) Neutrophil Subset Dictates Breast Cancer Lung Metastasis via CD8(+) T Cell Death.
Ly6g(高)中性粒细胞亚群通过CD8(+)T细胞死亡决定乳腺癌肺转移。
Microplastic-Induced Macrophage Dysfunction Drives Lung Tumor Progression through Glutathione Imbalance.
微塑料诱导的巨噬细胞功能障碍通过谷胱甘肽失衡驱动肺肿瘤进展。
Escherichia coli promotes colorectal cancer metastasis by maintaining enhancer-promoter loops through releasing neutrophil extracellular traps.
大肠杆菌通过释放中性粒细胞胞外陷阱来维持增强子-启动子环,从而促进结直肠癌转移。
Loss of Fsr quorum sensing promotes biofilm formation and worsens outcomes in enterococcal infective endocarditis.
Fsr 群体感应的丧失会促进生物膜的形成,并使肠球菌感染性心内膜炎的预后恶化。
Clostridium perfringens alpha toxin drives pathological NETosis via immature neutrophil mobilization and functional reprogramming
产气荚膜梭菌α毒素通过动员未成熟中性粒细胞和功能重编程驱动病理性NETosis
Bifidobacterium Breve Yang08 Alleviates Atopic Dermatitis By Enriching Akkermansia Muciniphila and Inhibiting Neutrophil Extracellular Traps Formation In Mice.
短双歧杆菌 Yang08 通过富集 Akkermansia Muciniphila 和抑制小鼠中性粒细胞胞外陷阱的形成来缓解特应性皮炎。
Dual targeting of AMRC12 and Malassezia globosa disrupts MYC liquid condensates-driven nuclear pore complex biogenesis in neuroblastoma.
双重靶向 AMRC12 和马拉色菌可破坏神经母细胞瘤中 MYC 液态凝聚物驱动的核孔复合体生物合成。
Mesenchymal stem cell transplantation alleviated TBI-induced lung injury by inhibiting PAD4-dependent NET formation.
间充质干细胞移植通过抑制 PAD4 依赖性 NET 形成来减轻 TBI 引起的肺损伤。
Gut microbiota dysbiosis exacerbates acute pancreatitis via Escherichia coli-driven neutrophil heterogeneity and NETosis.
肠道菌群失调通过大肠杆菌驱动的中性粒细胞异质性和NETosis加剧急性胰腺炎。
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