产品: IRX2 抗体
货号: AF0552
描述: Rabbit polyclonal antibody to IRX2
应用: WB IHC IF/ICC
反应: Human, Mouse, Rat
预测: Pig, Horse, Rabbit, Dog
分子量: 50kDa; 49kD(Calculated).
蛋白号: Q9BZI1
RRID: AB_2834315

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 50ul RMB¥ 1250 现货
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 200ul RMB¥ 3000 现货

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产品描述

来源:
Rabbit
应用:
WB 1:500-1:2000, 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
预测:
Pig(100%), Horse(100%), Rabbit(100%), Dog(100%)
克隆:
Polyclonal
特异性:
IRX2 Antibody detects endogenous levels of total IRX2.
RRID:
AB_2834315
引用格式: Affinity Biosciences Cat# AF0552, RRID:AB_2834315.
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

Homeodomain protein IRXA2; Iroquois homeobox 2; Iroquois homeobox protein 2; Iroquois-class homeodomain protein irx-2; IRX 2; irx2; IRX2_HUMAN; IrxA2;

抗原和靶标

免疫原:
Uniprot:
基因/基因ID:
描述:
IRX1 is a member of the Iroquois homeobox gene family. Members of this family appear to play multiple roles during pattern formation of vertebrate embryos.
序列:
MSYPQGYLYQAPGSLALYSCPAYGASALAAPRSEELARSASGSAFSPYPGSAAFTAQAATGFGSPLQYSADAAAAAAGFPSYMGAPYDAHTTGMTGAISYHPYGSAAYPYQLNDPAYRKNATRDATATLKAWLNEHRKNPYPTKGEKIMLAIITKMTLTQVSTWFANARRRLKKENKMTWAPRNKSEDEDEDEGDATRSKDESPDKAQEGTETSAEDEGISLHVDSLTDHSCSAESDGEKLPCRAGDPLCESGSECKDKYDDLEDDEDDDEEGERGLAPPKPVTSSPLTGLEAPLLSPPPEAAPRGGRKTPQGSRTSPGAPPPASKPKLWSLAEIATSDLKQPSLGPGCGPPGLPAAAAPASTGAPPGGSPYPASPLLGRPLYYTSPFYGNYTNYGNLNAALQGQGLLRYNSAAAAPGEALHTAPKAASDAGKAGAHPLESHYRSPGGGYEPKKDASEGCTVVGGGVQPYL

种属预测

种属预测:

score>80的预测可信度较高,可尝试用于WB检测。*预测模型主要基于免疫原序列比对,结果仅作参考,不作为质保凭据。

Species
Results
Score
Pig
100
Horse
100
Dog
100
Rabbit
100
Chicken
67
Bovine
0
Sheep
0
Xenopus
0
Zebrafish
0
Model Confidence:
High(score>80) Medium(80>score>50) Low(score<50) No confidence

翻译修饰 - Q9BZI1 作为底物

Site PTM Type Enzyme
S46 Phosphorylation P28482 (MAPK1)
S64 Phosphorylation P28482 (MAPK1)
S186 Phosphorylation
S231 Phosphorylation
S233 Phosphorylation
S236 Phosphorylation
S252 Phosphorylation
S254 Phosphorylation
T310 Phosphorylation
S317 Phosphorylation P27361 (MAPK3)
S325 Phosphorylation
S338 Phosphorylation

研究背景

细胞定位:

Nucleus.

Extracellular region or secreted Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi apparatus Nucleus Mitochondrion Manual annotation Automatic computational assertionSubcellular location
蛋白家族:

Belongs to the TALE/IRO homeobox family.

文献引用

1). IRX2 regulates angiotensin II-induced cardiac fibrosis by transcriptionally activating EGR1 in male mice. Nature Communications (PubMed: 37587150) [IF=16.6]

Application: WB    Species: Mouse    Sample: cardiac fibroblasts

Fig. 1 IRX2 expression was increased in fibrotic hearts. A Relative mRNA levels of 6 Irx family members in adult mouse cardiac fibroblasts (CFs) after angiotensin II (Ang II) treatment for 24 h (n = 5). B Relative mRNA levels of 6 IRX family members in human CFs after Ang II treatment for 24 h (n = 5). C Irx2 mRNA levels in the heart after Ang II infusion by an osmotic minipump (n = 6). D Representative western blots and statistical analysis of IRX2 expression in the heart after Ang II infusion for 12 weeks (n = 6). E Representative western blots and statistical analysis of IRX2 expression in heart samples obtained from patients with dilated cardiomyopathy (DCM) and control (Con) donors (Con, n = 6; DCM, n = 7). F Irx2 mRNA levels in endothelial cells (ECs), cardiomyocytes (CMs) and CFs isolated from hearts infused with Ang II for 12 weeks (n = 6). G Representative western blots and quantification of IRX2 protein expression in CFs isolated from hearts infused with Ang II for 12 weeks (n = 6). Data are shown as the mean ± SEM, and analysed using an unpaired two-tailed Student′s t test. For the analysis in (C), one-way ANOVA with Tamhane’s T2 test was conducted. Source data are provided as a Source Data file.

Application: IF/ICC    Species: Mouse    Sample: cardiac fibroblasts

Fig. 2 Conditional fibroblast-specific Irx2-deficient mice exhibited attenuated fibrotic remodelling in response to angiotensin II (Ang II) infusion. A Conditional fibroblast-specific Irx2-deficient mice (Irx2 cfKO) were bred by crossing mice with a conditional knockout allele of Irx2 (Irx2fl/fl) with Col1α2-Cre mice. Irx2 cfKO mice and littermate controls were subjected to Ang II infusion for 12 weeks. B Representative western blots and statistical analysis of IRX2 protein expression in CFs isolated from Irx2 cfKO mice and littermate controls (n = 5). C–E Irx2 cfKO mice exhibited an attenuated heart weight-to-tibia length (HW/TL) ratio (n = 10 mice, Col1α2-Cre+Saline; n = 12 mice, Irx2fl/fl+Saline; n = 12 mice, Irx2 cfKO+Saline; n = 12 mice, Col1α2-Cre+Ang II; n = 11 mice, Irx2fl/fl+Ang II; n = 12 mice, Irx2 cfKO+Ang II) (C), a reduced fibrosis area (n = 5) (D), and a decreased cell area of cardiomyocytes (n = 5) (E) after Ang II infusion. F Relative mRNA levels of Col1 and Col3 in hearts from Irx2 cfKO mice and littermate controls after Ang II infusion (n = 6). G Cardiac function (n = 6) was improved in Ang II-infused Irx2 cfKO mice. Data are shown as the mean ± SEM, and analysed using one-way ANOVA followed by Tukey post hoc test (E and G) or Tamhane’s T2 test (C, D and F). For the analysis in (B), an unpaired two-tailed Student′s t test was conducted. Source data are provided as a Source Data file.

Application: IHC    Species: Mouse    Sample: cardiac fibroblasts

Fig. 2 Conditional fibroblast-specific Irx2-deficient mice exhibited attenuated fibrotic remodelling in response to angiotensin II (Ang II) infusion. A Conditional fibroblast-specific Irx2-deficient mice (Irx2 cfKO) were bred by crossing mice with a conditional knockout allele of Irx2 (Irx2fl/fl) with Col1α2-Cre mice. Irx2 cfKO mice and littermate controls were subjected to Ang II infusion for 12 weeks. B Representative western blots and statistical analysis of IRX2 protein expression in CFs isolated from Irx2 cfKO mice and littermate controls (n = 5). C–E Irx2 cfKO mice exhibited an attenuated heart weight-to-tibia length (HW/TL) ratio (n = 10 mice, Col1α2-Cre+Saline; n = 12 mice, Irx2fl/fl+Saline; n = 12 mice, Irx2 cfKO+Saline; n = 12 mice, Col1α2-Cre+Ang II; n = 11 mice, Irx2fl/fl+Ang II; n = 12 mice, Irx2 cfKO+Ang II) (C), a reduced fibrosis area (n = 5) (D), and a decreased cell area of cardiomyocytes (n = 5) (E) after Ang II infusion. F Relative mRNA levels of Col1 and Col3 in hearts from Irx2 cfKO mice and littermate controls after Ang II infusion (n = 6). G Cardiac function (n = 6) was improved in Ang II-infused Irx2 cfKO mice. Data are shown as the mean ± SEM, and analysed using one-way ANOVA followed by Tukey post hoc test (E and G) or Tamhane’s T2 test (C, D and F). For the analysis in (B), an unpaired two-tailed Student′s t test was conducted. Source data are provided as a Source Data file.

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