By Research Area
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Mouse Anti-ASB9 Recombinant Antibody (1D8) (CBMAB-A0529-LY)
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Mouse Anti-ATP5F1A Recombinant Antibody (51) (CBMAB-A4043-YC)
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Mouse Anti-C1QC Recombinant Antibody (CBFYC-0600) (CBMAB-C0654-FY)
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Mouse Anti-C5B-9 Recombinant Antibody (CBFYA-0216) (CBMAB-X0304-FY)
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Mouse Anti-CD247 Recombinant Antibody (6B10.2) (CBMAB-C1583-YY)
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Mouse Anti-ATP1A2 Recombinant Antibody (M7-PB-E9) (CBMAB-A4013-YC)
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Rabbit Anti-CCN1 Recombinant Antibody (CBWJC-3580) (CBMAB-C4816WJ)
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Mouse Anti-FN1 Monoclonal Antibody (D6) (CBMAB-1240CQ)
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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