产品: NUCL 抗体
货号: DF12542
描述: Rabbit polyclonal antibody to NUCL
应用: WB IHC IF/ICC
文献验证: WB
反应: Human, Mouse, Rat
预测: Pig, Sheep, Rabbit, Dog, Xenopus
蛋白号: P19338
RRID: AB_2845504

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   规格 价格 库存
 100ul RMB¥ 2300 现货
 200ul RMB¥ 3000 现货

货期: 当天发货

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产品描述

来源:
Rabbit
应用:
WB 1:500-1:2000, IF/ICC 1:100-1:500, IHC 1:50-1:200
*The optimal dilutions should be determined by the end user.
*Tips:

WB: 适用于变性蛋白样本的免疫印迹检测. IHC: 适用于组织样本的石蜡(IHC-p)或冰冻(IHC-f)切片样本的免疫组化/荧光检测. IF/ICC: 适用于细胞样本的荧光检测. ELISA(peptide): 适用于抗原肽的ELISA检测.

反应:
Human, Mouse, Rat
克隆:
Polyclonal
特异性:
NUCL Antibody detects endogenous levels of total NUCL.
RRID:
AB_2845504
引用格式: Affinity Biosciences Cat# DF12542, RRID:AB_2845504.
偶联:
Unconjugated.
纯化:
The antiserum was purified by peptide affinity chromatography using SulfoLink™ Coupling Resin (Thermo Fisher Scientific).
保存:
Rabbit IgG in phosphate buffered saline , pH 7.4, 150mM NaCl, 0.02% sodium azide and 50% glycerol. Store at -20 °C. Stable for 12 months from date of receipt.
别名:

展开/折叠

C23; FLJ45706; MS1116; NCL; Nucl; NUCL_HUMAN; Nucleolin; Protein C23;

抗原和靶标

免疫原:

A synthesized peptide derived from human NUCL, corresponding to a region within the internal amino acids.

基因/基因ID:

研究领域

· Human Diseases > Infectious diseases: Bacterial > Pathogenic Escherichia coli infection.

文献引用

1). A novel lncRNA SNHG29 regulates EP300- related histone acetylation modification and inhibits FLT3-ITD AML development. Leukemia, 2023 (PubMed: 37157016) [IF=12.8]

2). Nucleolin Malonylation as a Nuclear-Cytosol Signal Exchange Mechanism to Drive Cell Proliferation in Hepatocarcinoma by Enhancing AKT Translation. The Journal of biological chemistry, 2024 (PubMed: 39305961) [IF=4.0]

3). Dimethyl itaconate inhibits LPS‑induced microglia inflammation and inflammasome‑mediated pyroptosis via inducing autophagy and regulating the Nrf‑2/HO‑1 signaling pathway. Molecular Medicine Reports, 2021 (PubMed: 34296312) [IF=3.4]

Application: WB    Species: Mice    Sample: microglial cells

Figure 5. DI regulates microglia inflammatory profile via inhibiting NF-κB phosphorylation and nuclear translocation. Levels of cytokines, including (A) iNOS, (B) TNF-α, (C) IL-6, (D) IFN-γ, (E) IL-18 and (F) IL-10, were determined by ELISA. (G) Nuclear translocation of p-NF-κB was determined by immunofluorescence staining. Scale bar, 100 µm. (H and I) p-NF-κB expression in the nucleus were determined by western blotting. (J and K) Ratio of whole cell p-NF-κB/total NF-κB expression was determined by western blotting. Data are presented as the mean ± standard error of the mean (n=3). **P<0.01, ***P<0.001 vs. sham group; #P<0.05, ##P<0.01, ###P<0.001 vs. LPS+ATP group. DI, dimethyl itaconate; iNOS, inducible nitric oxide synthase; LPS, lipopolysaccharide; p-, phosphorylated.

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