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Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Additionally we are shipping HIST1H1C Antibodies (37) and HIST1H1C Proteins (5) and many more products for this protein.
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Histone H1.2-T165 post translational modifications are dispensable for chromatin binding and cell proliferation while the H1.4-K26 (show KRT26 ELISA Kits) modifications are essential for proper cell cycle progression.
H1.2 interacts with Cul4A (show CUL4A ELISA Kits) and PAF1 (show PEX2 ELISA Kits) to activate developmental regulatory genes.
H1.2 is less abundant than other histone H1 (show H1F0 ELISA Kits) variants at the transcription start sites of inactive genes, and promoters enriched in H1.2 are different from those enriched in other histone H1 (show H1F0 ELISA Kits) variants and tend to be repressed.
Mutations in linker histone genes HIST1H1 B, C, D, and E; OCT2 (POU2F2); IRF8; and ARID1A underlying the pathogenesis of follicular lymphoma.
These data suggest that p53 (show TP53 ELISA Kits) acetylation-H1.2 phosphorylation cascade serves as a unique mechanism for triggering p53 (show TP53 ELISA Kits)-dependent DNA damage response pathways.
confirmed N-terminal acetylation on all isoforms plus a single internal acetylation site; phosphorylation sites were located on peptides containing the cyclin dependent kinase (show CDK1 ELISA Kits) (CDK (show CDK4 ELISA Kits)) consensus motif
The binding of histone H1 (show H1F0 ELISA Kits) to a general amyloid-like motif indicates that histone H1 (show H1F0 ELISA Kits) may play an important common role in diseases associated with amyloid-like fibrils.
Histone H1.2 was translocated from the nucleus to the mitochondria after treatment with bleomycin and co-localized with Bak (show BAK1 ELISA Kits) in mitochondria.
that the recruitment of YB1 (show YBX1 ELISA Kits), PURalpha (show PURA ELISA Kits), and H1.2 to the p53 (show TP53 ELISA Kits) target gene Bax (show BAX ELISA Kits) is required for repression of p53 (show TP53 ELISA Kits)-induced transcription.
Histone H1c gene expression is developmentally up-regulated to promote facultative heterochromatin in mature rod photoreceptors.
These results integrate the localization of an understudied type of chromatin proteins, namely the H1 variants, into the epigenome map of mouse ESCs (show NR2E3 ELISA Kits).
The N-terminal domain contributes toward the differential chromatin binding affinity, whereas the C-terminal domain contributes toward distinct nucleosomal interface of isotypes H10 (show H1F0 ELISA Kits) and H1c.
The amount of the linker histone H1c is strongly reduced in nuclear extracts of SCA7 (show ATXN7 ELISA Kits) retinas and that the cellular distribution of H1c is particularly altered in the facultative heterochromatin compartment.
The modular pattern of DNA methylation (show HELLS ELISA Kits) in the Ig heavy chain locus and histone modifications appears to be determined by at least 2 factors: the B-cell-specific transcription factor Pax5 (show PAX5 ELISA Kits) and linker histone H1 (show H1F0 ELISA Kits).
These observations reveal a mode of p53 (show TP53 ELISA Kits) regulation mediated by CHD8 (show CHD8 ELISA Kits), which may set a threshold for induction of apoptosis during early embryogenesis by counteracting p53 (show TP53 ELISA Kits) function through recruitment of histone H1 (show H1F0 ELISA Kits).
H1 isoforms H1.0, H1.1, and H1.2 are non-responsive to hormone whereas prolonged dexamethasone treatment effectively dephosphorylated the H1.3, H1.4, and H1.5 isoforms
Histones are basic nuclear proteins responsible for nucleosome structure of the chromosomal fiber in eukaryotes. Two molecules of each of the four core histones (H2A, H2B, H3, and H4) form an octamer, around which approximately 146 bp of DNA is wrapped in repeating units, called nucleosomes. The linker histone, H1, interacts with linker DNA between nucleosomes and functions in the compaction of chromatin into higher order structures. This gene is intronless and encodes a member of the histone H1 family. Transcripts from this gene lack polyA tails but instead contain a palindromic termination element. This gene is found in the large histone gene cluster on chromosome 6.
, histone H1.1
, histone H1.2
, histone H1d
, histone 1, H1c
, histone H1.11L
, H1 histone family, member 2
, histone H1c
, histone H1s-1
, H1 VAR.1
, histone H1
, H1 histone family, member 4
, Histone 1d
, histone H1.4