LI-COR P/N 926-42218,RRID AB_2814903,标准化的组蛋白 H3 小鼠单克隆抗体

Reagents > Histone H3 Mouse Monoclonal Antibody for Normalization

Histone H3 Mouse Monoclonal Antibody for Normalization

The Histone H3 primary antibody can be used as an internal loading control for normalization and is particularly effective when detecting target proteins in nuclear extracts.

The expression of Histone H3, or any housekeeping protein (HKP), should be validated to ensure that its expression does not change under experimental conditions.

Once validated, Histone H3 primary antibodies can be used for the detection of Histone H3 when performing multiplex Western blot detection.

Detect Histone H3 Mouse Monoclonal Antibody with IRDye® Goat anti-Mouse or IRDye Donkey anti-Mouse secondary antibodies.

组蛋白 H3 一抗可用作标准化的内部上样对照,在检测核提取物中的靶蛋白时特别有效。

应验证组蛋白 H3 或任何管家蛋白 (HKP) 的表达,以确保其表达在实验条件下不会改变。

经验证后,在进行多重蛋白质印迹检测时,组蛋白 H3 一抗可用于检测组蛋白 H3。

使用 IRDye® 山羊抗小鼠或 IRDye 驴抗小鼠二抗检测组蛋白 H3 小鼠单克隆抗体。

Other options for housekeeping protein normalization

Reactivity and Specificity

Histone H3 antibody is supplied in 10 mM HEPES (pH 7.5), 150 mM NaCl, 100 µg/mL BSA, 50% glycerol, and <0.02% sodium azide.

组蛋白 H3 抗体以 10 mM HEPES (pH 7.5)、150 mM NaCl、100 µg/mL BSA、50% 甘油和 <0.02% 叠氮化钠的形式提供。

Do not aliquot the antibody.

Properties Histone H3 Mouse Monoclonal Antibody (P/N 926-42218)
Species Cross-Reactivity Human, mouse, rat, monkey
Target Molecular Weight 17 kDa
Isotype Mouse IgG3
Specificity/Sensitivity Detects endogenous levels of total Histone H3 protein
Immunogen A peptide that is specific to the carboxy terminus of human histone H3 protein
Tested Applications Western blot (WB), Immunohistochemistry (IHC), Immunofluorescence (IF), Flow Cytometry (F), Chromatin Immunoprecipitation (CHIP)

蛋白质印迹 (WB)、免疫组织化学 (IHC)、免疫荧光 (IF)、流式细胞术 (F)、染色质免疫沉淀 (CHIP)

RRID

  • P/N 926-42218: RRID AB_2814903

Detection of Histone H3 Mouse Monoclonal Antibody in HeLa, NIH/3T3, and COS-7 Lysates

Histone H3 Mouse Monoclonal Antibody for Normalization
Histone H3 Mouse Monoclonal Antibody detected in HeLa, NIH/3T3, and COS-7 Lysates. Lysates were diluted from 2.5 μg to 156 ng. Lysates were separated on 4-12% Bis-Tris gels, electrophoresed at 200V for 45 minutes in MES Running Buffer, and transferred to nitrocellulose membranes in Tris-Glycine buffer at 100V for 65 minutes. Blots were blocked with Intercept® (PBS) Protein-Free Blocking Buffer (P/N 927-90001), probed with Histone H3 Mouse Monoclonal Antibody, and detected on an Odyssey® CLx Imager.
在 HeLa、NIH/3T3 和 COS-7 裂解物中检测到组蛋白 H3 小鼠单克隆抗体。 裂解物从 2.5 μg 稀释至 156 ng。 在 4-12% Bis-Tris 凝胶上分离裂解物,在 MES Running Buffer 中以 200V 电泳 45 分钟,然后在 100V 的 Tris-Glycine 缓冲液中转移至硝酸纤维素膜 65 分钟。 印迹用 Intercept® (PBS) 无蛋白封闭缓冲液(P/N 927-90001)封闭,用组蛋白 H3 小鼠单克隆抗体探测,并在 Odyssey® CLx 成像仪上检测。