By Research Area
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Rabbit Anti-B2M Recombinant Antibody (CBYY-0059) (CBMAB-0059-YY)
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Rat Anti-C5AR1 Recombinant Antibody (8D6) (CBMAB-C9139-LY)
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Mouse Anti-ATG5 Recombinant Antibody (9H197) (CBMAB-A3945-YC)
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Mouse Anti-FOXL1 Recombinant Antibody (CBXF-0845) (CBMAB-F0462-CQ)
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Armenian hamster Anti-CD40 Recombinant Antibody (HM40-3) (CBMAB-C10365-LY)
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Mouse Anti-EPO Recombinant Antibody (CBFYR0196) (CBMAB-R0196-FY)
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Mouse Anti-AGO2 Recombinant Antibody (V2-634169) (CBMAB-AP203LY)
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Rabbit Anti-Acetyl-Histone H3 (Lys36) Recombinant Antibody (V2-623395) (CBMAB-CP0994-LY)
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Mouse Anti-ASTN1 Recombinant Antibody (H-9) (CBMAB-1154-CN)
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Mouse Anti-BIRC7 Recombinant Antibody (88C570) (CBMAB-L0261-YJ)
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Mouse Anti-AMIGO2 Recombinant Antibody (CBYY-C0756) (CBMAB-C2192-YY)
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Mouse Anti-ACTN4 Recombinant Antibody (V2-6075) (CBMAB-0020CQ)
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Mouse Anti-ASH1L Monoclonal Antibody (ASH5H03) (CBMAB-1372-YC)
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Mouse Anti-ACVR1C Recombinant Antibody (V2-179685) (CBMAB-A1041-YC)
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Mouse Anti-DMPK Recombinant Antibody (CBYCD-324) (CBMAB-D1200-YC)
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Rat Anti-4-1BB Recombinant Antibody (V2-1558) (CBMAB-0953-LY)
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Mouse Anti-CCT6A/B Recombinant Antibody (CBXC-0168) (CBMAB-C5570-CQ)
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Mouse Anti-CD2AP Recombinant Antibody (BR083) (CBMAB-BR083LY)
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Rabbit Anti-ENO2 Recombinant Antibody (BA0013) (CBMAB-0272CQ)
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Rat Anti-(1-5)-α-L-Arabinan Recombinant Antibody (V2-501861) (CBMAB-XB0003-YC)
Epigenetics Research
For an extended period, the central dogma positioned the DNA sequence as the definitive repository of biological information. This paradigm, however, has been profoundly expanded by the emergence of epigenetics, a field elucidating a complex super-genomic regulatory network that governs the interpretation of the genetic blueprint itself. Fundamentally, epigenetics refers to heritable alterations in gene expression, transmitted through mitosis and in some cases meiosis, that occur without modifications to the primary DNA sequence. The orchestration of gene expression through these mechanisms is now understood to be indispensable for fundamental processes, including the establishment of cellular identity during differentiation, organismal development, and the dynamic response of an organism to its environment.
The molecular basis of epigenetic regulation involves several interconnected mechanisms. Key among these are the covalent methylation of DNA, a canonical silencing mark, and a vast repertoire of post-translational modifications (PTMs) to histone proteins. These PTMs, notably acetylation and methylation, dynamically alter chromatin architecture. For instance, acetylation typically yields a relaxed, transcriptionally permissive euchromatic state, whereas specific methylation marks like H3K9me3 and H3K27me3 promote the formation of compact, inert heterochromatin. The combinatorial interplay of these modifications, influenced by non-coding RNAs, is speculated to form a sophisticated 'epigenetic code,' enabling a highly nuanced regulatory framework.
Understanding epigenetic pathways has transcended academic pursuit to become a critical frontier in disease research. A growing body of evidence now implicates dysregulated epigenetic landscapes as a central pathological feature in a wide spectrum of human diseases. This includes various malignancies and a range of neurodegenerative and metabolic disorders, where aberrant epigenetic marks are now considered critical hallmarks. To empower your research, Creative Biolabs offers a comprehensive portfolio of highly validated antibodies targeting key epigenetic players, including specific histone modifications and DNA methyltransferases. Let us provide the precise tools you need to decipher the epigenetic code and unlock new therapeutic possibilities.
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