Human Histone H3 (acetyl K27) peptide
Human Histone H3 (acetyl K27) peptide
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(1 Publication)
Human Histone H3 (acetyl K27) peptide is a Synthetic blocking peptide. >90% and suitable for Dot, BL.
別名を表示する
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, H3FC, HIST1H3C, H3C1, 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, H3K27ac
- WB
Project3498****
Western blot - Human Histone H3 (acetyl K27) peptide (AB24404)
All lanes:
Anti-Histone H3 (acetyl K23) antibody (ab47813) at 1 µg/mL
Lanes 1, 4, 7 and 8:
HeLa Histone Preparation Nuclear Lysate - Butyrated at 2.5 µg
Lane 2:
HeLa Histone Preparation Nuclear Lysate - Butyrated at 2.5 µg with Human Histone H3 peptide (ab17163)
Lane 3:
HeLa Histone Preparation Nuclear Lysate - Butyrated at 2.5 µg with Histone H3 peptide - acetyl K36
Lane 5:
HeLa Histone Preparation Nuclear Lysate - Butyrated at 2.5 µg with Histone H3 peptide - acetyl K14
Lane 6:
HeLa Histone Preparation Nuclear Lysate - Butyrated at 2.5 µg with Human Histone H3 (acetyl K18) peptide (ab24003)
Secondary
All lanes:
IRDye 680 Conjugated Goat Anti-Rabbit IgG (H+L) at 1/10000 dilution
false
- WB
Ap796247****
Western blot - Human Histone H3 (acetyl K27) peptide (AB24404)
All lanes:
Western blot - Anti-Histone H3 (acetyl K18) antibody - ChIP Grade (<a href='/products/primary-antibodies/histone-h3-acetyl-k18-antibody-chip-grade-ab1191'>ab1191</a>) at 1 µg/mL
Lanes 1, 3, 6, 7 and 9:
HeLa Histone Preparation Nuclear Lysate at 2.5 µg
Lane 2:
HeLa Histone Preparation Nuclear Lysate at 2.5 µg with Histone H3 peptide - unmodified R17
Lane 4:
HeLa Histone Preparation Nuclear Lysate at 2.5 µg with Histone H3 peptide - acetyl K14
Lane 5:
HeLa Histone Preparation Nuclear Lysate at 2.5 µg with Human Histone H3 (acetyl K18) peptide (ab24003)
Lane 8:
HeLa Histone Preparation Nuclear Lysate at 2.5 µg with Histone H3 peptide - acetyl K36
Secondary
All lanes:
Goat polyclonal to Rabbit IgG - H&L - Pre-Adsorbed (HRP) at 1/3000 dilution
Predicted band size: 15 kDa
Observed band size: 17 kDa
true
Exposure time: 1min
- WB
Project4020****
Western blot - Human Histone H3 (acetyl K27) peptide (AB24404)
All lanes:
Western blot - Anti-Histone H3 (acetyl K9) antibody - ChIP Grade (<a href='/products/primary-antibodies/histone-h3-acetyl-k9-antibody-chip-grade-ab10812'>ab10812</a>) at 1 µg/mL
Lanes 1, 2, 3, 6 and 7:
Calf Thymus Histone Preparation Nuclear Lysate at 0.5 µg
Lane 4:
Calf Thymus Histone Preparation Nuclear Lysate at 0.5 µg with Histone H3 peptide - acetyl K14
Lane 5:
Calf Thymus Histone Preparation Nuclear Lysate at 0.5 µg with Human Histone H3 (acetyl K18) peptide (ab24003)
Secondary
All lanes:
Goat polyclonal to Rabbit IgG - H&L - Pre-Adsorbed (HRP) at 1/5000 dilution
Predicted band size: 15 kDa
Observed band size: 17 kDa
true
Exposure time: 30s
- WB
Unknown
Western blot - Human Histone H3 (acetyl K27) peptide (AB24404)
ab4729 specifically recognises acetyl K27 histone H3 in calf thymus histone lysate, which is specifically blocked using the immunizing peptide ab24404.
Lanes 1 and 3:
Western blot - Anti-Histone H3 (acetyl K27) antibody - ChIP Grade (<a href='/products/primary-antibodies/histone-h3-acetyl-k27-antibody-chip-grade-ab4729'>ab4729</a>) at 0.2 µg/mL
Lanes 2 and 4:
Western blot - Anti-Histone H3 (acetyl K27) antibody - ChIP Grade (<a href='/products/primary-antibodies/histone-h3-acetyl-k27-antibody-chip-grade-ab4729'>ab4729</a>) at 0.1 µg/mL
All lanes:
Calf thymus histone lysate at 1 µg
Secondary
All lanes:
Goat anti-rabbit (HRP) at 1/2000 dilution
Predicted band size: 15 kDa
false
- Dot
AbReview21276****
Dot Blot - Human Histone H3 (acetyl K27) peptide (AB24404)
ab24404 (at 0.01 and 0.1 μg) used in Dot Blot to test for cross-reactivity of ab4729 (1/2500). An HRP-conjugated Mouse anti-rabbit polyclonal (1/10000) was used as the secondary antibody.
This image is courtesy of an anonymous Abreview
Reactivity data
製品の詳細
- If the peptide doesn't dissolve try an organic solvent e.g. DMSO, then dilute using water or buffer.
- Consider that any solvent used must be compatible with your assay. If a peptide does not dissolve and you need to recover it, lyophilise to remove the solvent.
- Gentle warming and sonication can effectively aid peptide solubilisation. If the solution is cloudy or has gelled the peptide may be in suspension rather than solubilised.
- Peptides containing cysteine are easily oxidised, so should be prepared in solution just prior to use.
配列情報
出荷温度及び保存条件
出荷温度
短期保存期間
短期保存温度
長期保存温度
分注に関する情報
保管に関する情報
製品の性状
製品の状態
Liquid
一般的な情報
機能
The protein expressed by gene H3C1 is a core component of the nucleosome, which is essential for wrapping and compacting DNA into chromatin. This process restricts DNA accessibility to cellular machineries that use DNA as a template. Consequently, histones are central to transcription regulation, DNA repair, DNA replication, and chromosomal stability. DNA accessibility is regulated through a complex set of post-translational modifications of histones, known as the histone code, and through nucleosome remodeling. This supplementary information is collated from multiple sources and compiled automatically.
配列の類似性
Belongs to the histone H3 family.
翻訳後修飾
Acetylation is generally linked to gene activation. Acetylation on Lys-10 (H3K9ac) impairs methylation at Arg-9 (H3R8me2s). Acetylation on Lys-19 (H3K18ac) and Lys-24 (H3K24ac) favors methylation at Arg-18 (H3R17me). Acetylation at Lys-123 (H3K122ac) by EP300/p300 plays a central role in chromatin structure: localizes at the surface of the histone octamer and stimulates transcription, possibly by promoting nucleosome instability.. Citrullination at Arg-9 (H3R8ci) and/or Arg-18 (H3R17ci) by PADI4 impairs methylation and represses transcription.. Asymmetric dimethylation at Arg-18 (H3R17me2a) by CARM1 is linked to gene activation. Symmetric dimethylation at Arg-9 (H3R8me2s) by PRMT5 is linked to gene repression. Asymmetric dimethylation at Arg-3 (H3R2me2a) by PRMT6 is linked to gene repression and is mutually exclusive with H3 Lys-5 methylation (H3K4me2 and H3K4me3). H3R2me2a is present at the 3' of genes regardless of their transcription state and is enriched on inactive promoters, while it is absent on active promoters.. Methylation at Lys-5 (H3K4me), Lys-37 (H3K36me) and Lys-80 (H3K79me) are linked to gene activation. Methylation at Lys-5 (H3K4me) facilitates subsequent acetylation of H3 and H4. Methylation at Lys-80 (H3K79me) is associated with DNA double-strand break (DSB) responses and is a specific target for TP53BP1. Methylation at Lys-10 (H3K9me) and Lys-28 (H3K27me) are linked to gene repression. Methylation at Lys-10 (H3K9me) is a specific target for HP1 proteins (CBX1, CBX3 and CBX5) and prevents subsequent phosphorylation at Ser-11 (H3S10ph) and acetylation of H3 and H4. Methylation at Lys-5 (H3K4me) and Lys-80 (H3K79me) require preliminary monoubiquitination of H2B at 'Lys-120'. Methylation at Lys-10 (H3K9me) and Lys-28 (H3K27me) are enriched in inactive X chromosome chromatin. Monomethylation at Lys-57 (H3K56me1) by EHMT2/G9A in G1 phase promotes interaction with PCNA and is required for DNA replication.. Phosphorylated at Thr-4 (H3T3ph) by VRK1 (PubMed:31527692). Phosphorylated at Thr-4 (H3T3ph) by HASPIN during prophase and dephosphorylated during anaphase (PubMed:15681610, PubMed:16185088). Phosphorylation at Ser-11 (H3S10ph) by AURKB is crucial for chromosome condensation and cell-cycle progression during mitosis and meiosis. In addition phosphorylation at Ser-11 (H3S10ph) by RPS6KA4 and RPS6KA5 is important during interphase because it enables the transcription of genes following external stimulation, like mitogens, stress, growth factors or UV irradiation and result in the activation of genes, such as c-fos and c-jun. Phosphorylation at Ser-11 (H3S10ph), which is linked to gene activation, prevents methylation at Lys-10 (H3K9me) but facilitates acetylation of H3 and H4. Phosphorylation at Ser-11 (H3S10ph) by AURKB mediates the dissociation of HP1 proteins (CBX1, CBX3 and CBX5) from heterochromatin. Phosphorylation at Ser-11 (H3S10ph) is also an essential regulatory mechanism for neoplastic cell transformation. Phosphorylated at Ser-29 (H3S28ph) by MAP3K20 isoform 1, RPS6KA5 or AURKB during mitosis or upon ultraviolet B irradiation. Phosphorylation at Thr-7 (H3T6ph) by PRKCB is a specific tag for epigenetic transcriptional activation that prevents demethylation of Lys-5 (H3K4me) by LSD1/KDM1A. At centromeres, specifically phosphorylated at Thr-12 (H3T11ph) from prophase to early anaphase, by DAPK3 and PKN1. Phosphorylation at Thr-12 (H3T11ph) by PKN1 or isoform M2 of PKM (PKM2) is a specific tag for epigenetic transcriptional activation that promotes demethylation of Lys-10 (H3K9me) by KDM4C/JMJD2C. Phosphorylation at Thr-12 (H3T11ph) by chromatin-associated CHEK1 regulates the transcription of cell cycle regulatory genes by modulating acetylation of Lys-10 (H3K9ac). Phosphorylation at Tyr-42 (H3Y41ph) by JAK2 promotes exclusion of CBX5 (HP1 alpha) from chromatin.. Monoubiquitinated by RAG1 in lymphoid cells, monoubiquitination is required for V(D)J recombination (By similarity). Ubiquitinated by the CUL4-DDB-RBX1 complex in response to ultraviolet irradiation. This may weaken the interaction between histones and DNA and facilitate DNA accessibility to repair proteins.. Lysine deamination at Lys-5 (H3K4all) to form allysine is mediated by LOXL2. Allysine formation by LOXL2 only takes place on H3K4me3 and results in gene repression.. Crotonylation (Kcr) is specifically present in male germ cells and marks testis-specific genes in post-meiotic cells, including X-linked genes that escape sex chromosome inactivation in haploid cells. Crotonylation marks active promoters and enhancers and confers resistance to transcriptional repressors. It is also associated with post-meiotically activated genes on autosomes.. Butyrylation of histones marks active promoters and competes with histone acetylation. It is present during late spermatogenesis.. Succinylation at Lys-80 (H3K79succ) by KAT2A takes place with a maximum frequency around the transcription start sites of genes (PubMed:29211711). It gives a specific tag for epigenetic transcription activation (PubMed:29211711). Desuccinylation at Lys-123 (H3K122succ) by SIRT7 in response to DNA damage promotes chromatin condensation and double-strand breaks (DSBs) repair (PubMed:27436229).. Serine ADP-ribosylation by PARP1 or PARP2 constitutes the primary form of ADP-ribosylation of proteins in response to DNA damage (PubMed:30257210, PubMed:34874266). Serine ADP-ribosylation at Ser-11 (H3S10ADPr) promotes recruitment of CHD1L (PubMed:34874266). H3S10ADPr is mutually exclusive with phosphorylation at Ser-11 (H3S10ph) and impairs acetylation at Lys-10 (H3K9ac) (PubMed:30257210).. Serotonylated by TGM2 at Gln-6 (H3Q5ser) during serotonergic neuron differentiation (PubMed:30867594). H3Q5ser is associated with trimethylation of Lys-5 (H3K4me3) and enhances general transcription factor IID (TFIID) complex-binding to H3K4me3, thereby facilitating transcription (PubMed:30867594).. Dopaminylated by TGM2 at Gln-6 (H3Q5dop) in ventral tegmental area (VTA) neurons (PubMed:32273471). H3Q5dop mediates neurotransmission-independent role of nuclear dopamine by regulating relapse-related transcriptional plasticity in the reward system (By similarity).. Lactylated in macrophages by EP300/P300 by using lactoyl-CoA directly derived from endogenous or exogenous lactate, leading to stimulates gene transcription.
細胞内局在性
Nucleus
ターゲットの情報
文献 (1)
Recent publications for all applications. Explore the full list and refine your search
Plant science : an international journal of experi 276:250-267 PubMed30348325
2018
Applications
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Species
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