Acetyl-Histone H3 (Lys14) 抗体 (YA643)(PBS only) (HY-P80529A)

H3K14ac; H3/j; H3C1; H3C2; H3C3; H3C4; H3C6; H3C7; H3C8; H3FJ; H3C10; H3C11; HIST1H3J

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反应种属：Human, Rat

抗原名称：Acetyl-Histone H3 (Lys14)

应用：WB, IF/ICC, IP

标记：Unconjugated

用户验证的应用详细信息背景信息

用户验证的应用

经验证应用

项目	详情
WB	Western blot analysis of extracts from Raji (lane 1) and Hela (lane 2) and NIH3T3 (lane 3) using Acetyl-Histone H3 (Lys14) antibody. Proteins were transferred to a PVDF membrane and blocked with 5% nonfat powdered milk in PBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (GAPDH, 1/3000) was diluted with 5% nonfat powdered milk in PBST at 4°C overnight. Goat Anti-Rabbit IgG-HRP Secondary Antibody (1/8,000) was incubated for 45min at room temperature.
ICC	Immunocytochemistry analysis of HepG2 cells labeling Acetyl-Histone H3 (Lys14) with Acetyl-Histone H3 (Lys14) Antibody ( HY-P80529 ) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with quick block buffer for 10 minutes at room temperature. Cells were then incubated with Acetyl-Histone H3 (Lys14) Antibody ( HY-P80529 ) at 1/100 dilution in quick block buffer overnight at 4 ℃. AF488-conjugated Goat Anti-Rabbit IgG H&L（HY-P8002, Green) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. The Nuclear counterstain was DAPI (Blue). Immunocytochemistry analysis of HepG2 cells labeling Acetyl-Histone H3 (Lys14) with Acetyl-Histone H3 (Lys14) Antibody ( HY-P80529 ) at 1/200 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with quick block buffer for 10 minutes at room temperature. Cells were then incubated with Acetyl-Histone H3 (Lys14) Antibody ( HY-P80529 ) at 1/200 dilution in quick block buffer overnight at 4 ℃. AF488-conjugated Goat Anti-Rabbit IgG H&L（HY-P8002, Green) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. The Nuclear counterstain was DAPI (Blue).

项目

详情

Western blot analysis of extracts from Raji (lane 1) and Hela (lane 2) and NIH3T3 (lane 3) using Acetyl-Histone H3 (Lys14) antibody. Proteins were transferred to a PVDF membrane and blocked with 5% nonfat powdered milk in PBST for 2 hour at room temperature. The primary antibody (1/1000) and Loading control antibody (GAPDH, 1/3000) was diluted with 5% nonfat powdered milk in PBST at 4°C overnight. Goat Anti-Rabbit IgG-HRP Secondary Antibody (1/8,000) was incubated for 45min at room temperature.

ICC

Immunocytochemistry analysis of HepG2 cells labeling Acetyl-Histone H3 (Lys14) with Acetyl-Histone H3 (Lys14) Antibody ( HY-P80529 ) at 1/100 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with quick block buffer for 10 minutes at room temperature. Cells were then incubated with Acetyl-Histone H3 (Lys14) Antibody ( HY-P80529 ) at 1/100 dilution in quick block buffer overnight at 4 ℃. AF488-conjugated Goat Anti-Rabbit IgG H&L（HY-P8002, Green) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. The Nuclear counterstain was DAPI (Blue). Immunocytochemistry analysis of HepG2 cells labeling Acetyl-Histone H3 (Lys14) with Acetyl-Histone H3 (Lys14) Antibody ( HY-P80529 ) at 1/200 dilution. Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 minutes at room temperature, then blocked with quick block buffer for 10 minutes at room temperature. Cells were then incubated with Acetyl-Histone H3 (Lys14) Antibody ( HY-P80529 ) at 1/200 dilution in quick block buffer overnight at 4 ℃. AF488-conjugated Goat Anti-Rabbit IgG H&L（HY-P8002, Green) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. The Nuclear counterstain was DAPI (Blue).

详细信息

免疫原Synthetic peptide corresponding to residues surrounding Lys14 of Human Human Histone H3.The exact sequence is proprietary to MCE.

宿主/亚型Rabbit / IgG

全称Acetyl-Histone H3 (Lys14) 抗体 (YA643)(PBS only)

理论分子量15 kDa

实际/观测分子量15 kDa 请注意：因蛋白存在修饰或聚体等情况，以实测为准，预测仅为参考。

产品形式液体

偶联物Non-conjugated

储存缓冲液Supplied in PBS, pH 7.4.

储存条件保存条件 & 期限: Stored at -20°C for 1 year. Avoid repeated freeze / thaw cycles. 运输条件: Shipping with blue ice.

纯化方式affinity purified

Gene ID8350 [ NCBI ]

UniProt IDP68431

背景信息

功能：乙酰化组蛋白 H3 是核小体的核心组分。核小体将 DNA 缠绕并压缩为染色质，限制了以 DNA 为模板的细胞机器对 DNA 的可及性。因此，组蛋白在转录调控、DNA 修复、DNA 复制和染色体稳定性中发挥核心作用。DNA 的可及性通过一系列复杂的组蛋白翻译后修饰 (也称为组蛋白密码) 以及核小体重塑来调控。亚细胞定位：细胞核；染色体亚基：核小体是由组蛋白八聚体组成，包含两个 H2A、两个 H2B、两个 H3 和两个 H4 分子，组装成一个 H3-H4 异源四聚体和两个 H2A-H2B 异源二聚体。该八聚体包裹约 147 bp 的 DNA。核小体与 TONSL、CHAF1A、CHAF1B、MCM2 和 DNAJC9 相互作用 (PubMed:33857403)。核小体还与 NASP 相互作用；NASP 是一种组蛋白伴侣，能够稳定并维持可溶性组蛋白 H3-H4 二聚体 (PubMed:22195965)。