产品: 磷酸化 VEGFR2 (Tyr996) 抗体
货号: AF8022
描述: Rabbit polyclonal antibody to Phospho-VEGFR2 (Tyr996)
应用: WB IHC IF/ICC
文献验证: WB
反应: Human, Mouse, Rat, Monkey
预测: Pig, Bovine, Sheep, Dog
蛋白号: P35968
RRID: AB_2840085

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 100ul RMB¥ 2800 现货
 200ul RMB¥ 3800 现货

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产品描述

来源:
Rabbit
应用:
WB 1:1000-3000, IHC 1:50-1:200, IF/ICC 1:100-1:500
*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, Monkey
克隆:
Polyclonal
特异性:
Phospho-VEGFR2 (Tyr996) Antibody detects endogenous levels of VEGFR2 only when phosphorylated at Tyr996.
RRID:
AB_2840085
引用格式: Affinity Biosciences Cat# AF8022, RRID:AB_2840085.
偶联:
Unconjugated.
纯化:
The antibody is from purified rabbit serum by affinity purification via sequential chromatography on phospho-peptide and non-phospho-peptide affinity columns.
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

CD309; CD309 antigen; EC 2.7.10.1; Fetal liver kinase 1; FLK-1; FLK1; FLK1, mouse, homolog of; Kdr; Kinase insert domain receptor (a type III receptor tyrosine kinase); Kinase insert domain receptor; KRD1; Ly73; Protein tyrosine kinase receptor FLK1; Protein-tyrosine kinase receptor flk-1; soluble VEGFR2; Tyrosine kinase growth factor receptor; Vascular endothelial growth factor receptor 2; VEGFR 2; VEGFR; VEGFR-2; VEGFR2; VGFR2_HUMAN;

抗原和靶标

免疫原:

A synthesized peptide derived from human VEGFR2 around the phosphorylation site of Tyr996.

基因/基因ID:

研究领域

· Cellular Processes > Cellular community - eukaryotes > Focal adhesion.   (View pathway)

· Environmental Information Processing > Signal transduction > MAPK signaling pathway.   (View pathway)

· Environmental Information Processing > Signal transduction > Ras signaling pathway.   (View pathway)

· Environmental Information Processing > Signal transduction > Rap1 signaling pathway.   (View pathway)

· Environmental Information Processing > Signaling molecules and interaction > Cytokine-cytokine receptor interaction.   (View pathway)

· Environmental Information Processing > Signal transduction > PI3K-Akt signaling pathway.   (View pathway)

· Human Diseases > Drug resistance: Antineoplastic > EGFR tyrosine kinase inhibitor resistance.

· Human Diseases > Cancers: Overview > Proteoglycans in cancer.

文献引用

1). Isoflurane and Sevoflurane Induce Cognitive Impairment in Neonatal Rats by Inhibiting Neural Stem Cell Development Through Microglial Activation, Neuroinflammation, and Suppression of VEGFR2 Signaling Pathway. NEUROTOXICITY RESEARCH, 2022 (PubMed: 35471722) [IF=2.9]

Application: WB    Species: Rat    Sample: hippocampus

Fig. 6 The protein expression levels of Nestin, Sox2, CD11b, IL-6, TNF-α and p-VEGFR2/VEGFR2 in the hippocampus (n = 8 each per group) were detected 5 days after isoflurane and sevoflurane anesthesia. A, B. The results revealed that isoflurane (p = 0.000, for Nestin; p = 0.000, for Sox2) and sevoflurane (p = 0.000, for Nestin; p = 0.000, for Sox2) inhibited the expression of Nestin and Sox2. Isoflurane inhibited the expression of Nestin or Sox2 compared to that of sevoflurane (p = 0.040, for Nestin; p = 0.010, for Sox2). Furthermore, isoflurane (p = 0.000, for IL-6; p = 0.000, for TNF-α; p = 0.000, for CD11b) and sevoflurane (p = 0.000, for IL-6; p = 0.000, for TNF-α; p = 0.000, for CD11b) increased the levels of IL-6, TNF-α and the microglial marker CD11b in hippocampus. C-F. Isoflurane (p = 0.000, for p-VEGFR2; p = 0.000, for p-VEGFR2/VEGFR2) and sevoflurane (p = 0.000, for p-VEGFR2; p = 0.000, for p-VEGFR2/VEGFR2) decreased the level of p-VEGFR2 and the ratio of p-VEGFR2/VEGFR2. Data are mean ± SEM. **p < 0.01, *p < 0.05

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