产品: 磷酸化 ITK (Tyr512) 抗体
货号: AF8072
描述: Rabbit polyclonal antibody to Phospho-ITK (Tyr512)
应用: WB IHC
文献验证: WB, IHC
反应: Human, Mouse, Rat
预测: Pig, Zebrafish, Bovine, Horse, Sheep, Rabbit, Dog
蛋白号: Q08881
RRID: AB_2840135

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   规格 价格 库存
 100ul RMB¥ 2800 现货
 200ul RMB¥ 3800 现货

货期: 当天发货

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产品描述

来源:
Rabbit
应用:
WB 1:1000-3000, IHC 1:50-1:200
*The optimal dilutions should be determined by the end user. For optimal experimental results, antibody reuse is not recommended.
*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:
Phospho-ITK (Tyr512) Antibody detects endogenous levels of ITK only when phosphorylated at Tyr512.
RRID:
AB_2840135
引用格式: Affinity Biosciences Cat# AF8072, RRID:AB_2840135.
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

EMT; Homolog of mouse T cell itk/tsk; IL 2 inducible T cell kinase; IL2 inducible T cell kinase; Interleukin 2 inducible T cell kinase; Itk; ITK_HUMAN; Kinase EMT; LPFS1; LYK; MGC126257; MGC126258; PSCTK 2; PSCTK2; T cell specific kinase; T-cell-specific kinase; TSK; Tyrosine protein kinase; Tyrosine protein kinase ITK/TSK; Tyrosine protein kinase Lyk; Tyrosine-protein kinase ITK/TSK; Tyrosine-protein kinase Lyk;

抗原和靶标

免疫原:

A synthesized peptide derived from human ITK around the phosphorylation site of Tyr512.

基因/基因ID:

研究领域

· Organismal Systems > Immune system > Chemokine signaling pathway.   (View pathway)

· Organismal Systems > Immune system > T cell receptor signaling pathway.   (View pathway)

· Organismal Systems > Immune system > Leukocyte transendothelial migration.   (View pathway)

文献引用

1). Interleukin-2-inducible T-cell kinase inhibition to block NF-κB signaling exerts anti-tumor effects and enhances chemotherapy in NK/T-cell lymphoma. Cancer letters, 2025 (PubMed: 40054659) [IF=9.1]

2). Interleukin-2-inducible T-cell kinase inhibition to block NF-κB signaling exerts anti-tumor effect and enhances chemotherapy in NK/T-cell lymphoma. Cancer letters, 2025 (PubMed: 40054659) [IF=9.1]

Application: WB    Species: human    Sample:

Fig. 1. ITK is overexpressed in NKTCL and elevated ITK expression is associated with poor survival. A ITK gene expression (mean ± SD) of normal NK cells (n = 13), NKTCL patient samples (n = 58) and NKTCL cell lines (n = 14) from GEO database. One-way ANOVA and Dunnett post hoc multiple comparisons were used. B, C Validation of ITK mRNA and protein expression in normal NK and NKTCL cell lines (NK-YS, KHYG-1, YT and YTS) using real-time PCR (normalized to GAPDH as internal control, mean ± SD) and immunoblotting analysis (GAPDH used as loading control). D The p-ITK(Tyr512) expression of NKTCL patient samples (n = 8), Scale bar = 100 μm, up panel was representative pictures of IHC and bottom panel was colored images from QuPath. Patients marked in red died at cutoff day. E Sankey diagram demonstrated the correlation between p-ITK(Tyr512) H-score (calculated by QuPath) of patient samples and clinical information. Patients with higher p-ITK(Tyr512) expression seemed to be resistant to ASP and to have shorter survival. F Kaplan–Meier curve for the OS of NKTCL patients (n = 32) in GSE90784 according to ITK mRNA expression (ITK low vs ITK high). The p value was calculated via Log-rank test. G Univariate analysis identified risk factors of available NKTCL patients in GSE90784 set (n = 25) and forward stepwise Cox regression was used. ITK mRNA expression was one of the independent adverse risk factors for OS in NKTCL. HR, hazard ratio. CI, confidence interval. OS, overall survival. For all data, ∗p < 0.05; ∗∗p < 0.01; ∗∗∗p < 0.001; ns (not statistically significant), p ≥ 0.05.

Application: IHC    Species: human    Sample:

Fig. 1. ITK is overexpressed in NKTCL and elevated ITK expression is associated with poor survival. A ITK gene expression (mean ± SD) of normal NK cells (n = 13), NKTCL patient samples (n = 58) and NKTCL cell lines (n = 14) from GEO database. One-way ANOVA and Dunnett post hoc multiple comparisons were used. B, C Validation of ITK mRNA and protein expression in normal NK and NKTCL cell lines (NK-YS, KHYG-1, YT and YTS) using real-time PCR (normalized to GAPDH as internal control, mean ± SD) and immunoblotting analysis (GAPDH used as loading control). D The p-ITK(Tyr512) expression of NKTCL patient samples (n = 8), Scale bar = 100 μm, up panel was representative pictures of IHC and bottom panel was colored images from QuPath. Patients marked in red died at cutoff day. E Sankey diagram demonstrated the correlation between p-ITK(Tyr512) H-score (calculated by QuPath) of patient samples and clinical information. Patients with higher p-ITK(Tyr512) expression seemed to be resistant to ASP and to have shorter survival. F Kaplan–Meier curve for the OS of NKTCL patients (n = 32) in GSE90784 according to ITK mRNA expression (ITK low vs ITK high). The p value was calculated via Log-rank test. G Univariate analysis identified risk factors of available NKTCL patients in GSE90784 set (n = 25) and forward stepwise Cox regression was used. ITK mRNA expression was one of the independent adverse risk factors for OS in NKTCL. HR, hazard ratio. CI, confidence interval. OS, overall survival. For all data, ∗p < 0.05; ∗∗p < 0.01; ∗∗∗p < 0.001; ns (not statistically significant), p ≥ 0.05.

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