ARG1 Antibody - #DF6657

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产品: ARG1 抗体
货号: DF6657
描述: Rabbit polyclonal antibody to ARG1
应用: WB IHC IF/ICC
反应: Human, Mouse, Rat
预测: Pig, Xenopus
分子量: 35kDa; 35kD(Calculated).
蛋白号: P05089
RRID: AB_2838619

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   规格 价格 库存
 50ul RMB¥ 1250 现货
 100ul RMB¥ 2300 现货
 200ul RMB¥ 3000 现货

货期: 当天发货

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MS Report
HPLC Report
MSDS
说明书
COA
实验方案
WB Handbook
IHC Protocol
IF/ICC Protocol

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(82%), Xenopus(83%)
克隆:
Polyclonal
特异性:
ARG1 Antibody detects endogenous levels of total ARG1.
RRID:
AB_2838619
引用格式: Affinity Biosciences Cat# DF6657, RRID:AB_2838619.
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

A I; Al; ARG 1; arg1; ARGI1_HUMAN; Arginase 1; Arginase liver; Arginase type I; Arginase, liver; Arginase-1; Arginase1; Liver type arginase; Liver-type arginase; Type I arginase;

抗原和靶标

免疫原:
Uniprot:

P05089(ARGI1_HUMAN) >>Visit HPA database.

基因/基因ID:
ARG1(383)
表达:
P05089 ARGI1_HUMAN:

Within the immune system initially reported to be selectively expressed in granulocytes (polymorphonuclear leukocytes [PMNs]) (PubMed:15546957). Also detected in macrophages mycobacterial granulomas (PubMed:23749634). Expressed in group2 innate lymphoid cells (ILC2s) during lung disease (PubMed:27043409).

描述:
Arginase catalyzes the hydrolysis of arginine to ornithine and urea. At least two isoforms of mammalian arginase exist (types I and II) which differ in their tissue distribution, subcellular localization, immunologic crossreactivity and physiologic function. The type I isoform encoded by this gene, is a cytosolic enzyme and expressed predominantly in the liver as a component of the urea cycle. Inherited deficiency of this enzyme results in argininemia, an autosomal recessive disorder characterized by hyperammonemia. Two transcript variants encoding different isoforms have been found for this gene.
序列:
MSAKSRTIGIIGAPFSKGQPRGGVEEGPTVLRKAGLLEKLKEQECDVKDYGDLPFADIPNDSPFQIVKNPRSVGKASEQLAGKVAEVKKNGRISLVLGGDHSLAIGSISGHARVHPDLGVIWVDAHTDINTPLTTTSGNLHGQPVSFLLKELKGKIPDVPGFSWVTPCISAKDIVYIGLRDVDPGEHYILKTLGIKYFSMTEVDRLGIGKVMEETLSYLLGRKKRPIHLSFDVDGLDPSFTPATGTPVVGGLTYREGLYITEEIYKTGLLSGLDIMEVNPSLGKTPEEVTRTVNTAVAITLACFGLAREGNHKPIDYLNPPK

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
Xenopus
83
Pig
82
Bovine
73
Sheep
73
Dog
73
Horse
64
Zebrafish
0
Chicken
0
Rabbit
0
Model Confidence:
High(score>80) Medium(80>score>50) Low(score<50) No confidence

翻译修饰 - P05089 作为底物

Site PTM Type Enzyme
S16 Phosphorylation
T29 Phosphorylation
K33 Ubiquitination
Y50 Phosphorylation
S62 Phosphorylation
S72 Phosphorylation
S94 Phosphorylation
S102 Phosphorylation
S107 Phosphorylation
S109 Phosphorylation
S163 Phosphorylation
T166 Phosphorylation
C168 S-Nitrosylation
S170 Phosphorylation
K191 Acetylation
S217 Phosphorylation
Y265 Phosphorylation
C303 S-Nitrosylation

研究背景

功能:

Key element of the urea cycle converting L-arginine to urea and L-ornithine, which is further metabolized into metabolites proline and polyamides that drive collagen synthesis and bioenergetic pathways critical for cell proliferation, respectively; the urea cycle takes place primarily in the liver and, to a lesser extent, in the kidneys.

Functions in L-arginine homeostasis in nonhepatic tissues characterized by the competition between nitric oxide synthase (NOS) and arginase for the available intracellular substrate arginine. Arginine metabolism is a critical regulator of innate and adaptive immune responses. Involved in an antimicrobial effector pathway in polymorphonuclear granulocytes (PMN). Upon PMN cell death is liberated from the phagolysosome and depletes arginine in the microenvironment leading to suppressed T cell and natural killer (NK) cell proliferation and cytokine secretion. In group 2 innate lymphoid cells (ILC2s) promotes acute type 2 inflammation in the lung and is involved in optimal ILC2 proliferation but not survival (By similarity). In humans, the immunological role in the monocytic/macrophage/dendritic cell (DC) lineage is unsure.

细胞定位:

Cytoplasm. Cytoplasmic granule.
Note: Localized in azurophil granules of neutrophils (PubMed:15546957).

Extracellular region or secreted Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi apparatus Nucleus Mitochondrion Manual annotation Automatic computational assertionSubcellular location
组织特异性:

Within the immune system initially reported to be selectively expressed in granulocytes (polymorphonuclear leukocytes [PMNs]). Also detected in macrophages mycobacterial granulomas. Expressed in group2 innate lymphoid cells (ILC2s) during lung disease.

亚基结构:

Homotrimer. Interacts with CMTM6.

蛋白家族:

Belongs to the arginase family.

研究领域

· Human Diseases > Infectious diseases: Parasitic > Amoebiasis.

· Metabolism > Amino acid metabolism > Arginine biosynthesis.

· Metabolism > Amino acid metabolism > Arginine and proline metabolism.

· Metabolism > Global and overview maps > Metabolic pathways.

· Metabolism > Global and overview maps > Biosynthesis of amino acids.

文献引用

1). Multifunctional Injectable Microspheres Containing "Naturally-Derived" Photothermal Transducer for Synergistic Physical and Chemical Treating of Acute Osteomyelitis through Sequential Immunomodulation. ACS nano, 2024 (PubMed: 38335113) [IF=17.1]
2). Opsonization Inveigles Macrophages Engulfing Carrier-Free Bilirubin/JPH203 Nanoparticles to Suppress Inflammation for Osteoarthritis Therapy. Advanced science (Weinheim, Baden-Wurttemberg, Germany), 2024 (PubMed: 38593402) [IF=15.1]
3). Opsonized nanoparticles target and regulate macrophage polarization for osteoarthritis therapy: A trapping strategy. Journal of Controlled Release, 2022 (PubMed: 35489544) [IF=10.8]
4). Aligned electrospun poly(l-lactide) nanofibers facilitate wound healing by inhibiting macrophage M1 polarization via the JAK-STAT and NF-κB pathways. JOURNAL OF NANOBIOTECHNOLOGY, 2022 (PubMed: 35883095) [IF=10.2]

Application: WB    Species: Mice    Sample:

Fig. 2 The effect of aligned nanofibers on macrophage polarization. A Phalloidin staining of macrophages on electrospun membranes. Actin is stained green, and the nucleus is stained blue. B Flow cytometric analysis of macrophages. C qPCR analysis of M2 polarization-related genes. D ELISA analysis of IL-4 secretion. E qPCR analysis of M1 polarization-related genes (*p < 0.05, **p < 0.01, ***p < 0.001, n = 3). F Western blot analysis of macrophage polarization-related proteins. G and H Immunofluorescence analysis of CD86 and CD206 expression in macrophages. CD86 and CD206 are stained red, and the nucleus is stained blue
5). Low-intensity pulsed ultrasound promotes skeletal muscle regeneration via modulating the inflammatory immune microenvironment. International Journal of Biological Sciences, 2023 (PubMed: 36923940) [IF=9.2]
6). CCL5 derived from tumor-associated macrophages promotes prostate cancer stem cells and metastasis via activating β-catenin/STAT3 signaling. Cell Death & Disease, 2020 (PubMed: 32300100) [IF=9.0]

Application: WB    Species: human    Sample: prostate cancer cells

Fig. 3 TAM-secreted CCL5 promoted the invasion of prostate cancer cells and the self-renewal of PCSCs. a, b The reliability of THP1-derived TAMs was validated by analyzing the macrophage surface markers. THP1 monocytes were induced differentiation into macrophages (M0) by 100 ng/ ml PMA treatment for 24 h, which were further transformed into M2 phenotype macrophages (TAMs) by 10 ng/ml IL-4 induction for 72 h. c, d The CM of THP1-derived TAMs significantly promoted EMT, migration and invasion of prostate cancer cells, while CCL5 NA could partly abrogate that. Scale bars represent 200 μm for wound healing assay images and 50 μm for transwell assay images. e The CM of THP1-derived TAMs significantly promoted the self-renewal of PCSCs, while CCL5 NA could partly abrogate that. All values are presented as the mean ± SD. n = 3, *p < 0.05, **p < 0.01.
7). Oesophageal squamous cell carcinoma–associated IL‐33 rewires macrophage polarization towards M2 via activating ornithine decarboxylase. CELL PROLIFERATION, 2021 (PubMed: 33305406) [IF=8.5]

Application: IF/ICC    Species: human    Sample: M2 macrophages

FIGURE 2|IL-33 skews M2 macrophage polarization. F, Immunofluorescence staining for IL-33–induced M2 macrophages (scale bar = 20 μm). The green signal represents the staining of activated ornithine decarboxylase, and the blue signal represents the DAPI-stained nuclei. *P < .05; **P < .01; ***P < .001. Bars indicate mean and SEM of triplicate experiments and show a representative experiment of at least 3 independent experiments performed for each panel

Application: WB    Species: human    Sample: M2 macrophages

FIGURE 4|IL-33 promotes M2 macrophage polarization via ornithine decarboxylase (ODC) activation.E, iNOS and ARG1 protein levels were determined by Western blot in IL-33–induced M2 macrophage with or without knocking down ODC. *P < .05; **P < .01; ***P < .001. Bars indicate mean and SEM of triplicate experiments and show a representative experiment of at least 3 independent experiments performed for each panel
8). XIAOPI formula inhibits the pre-metastatic niche formation in breast cancer via suppressing TAMs/CXCL1 signaling. Cell Communication and Signaling, 2020 (PubMed: 32213179) [IF=8.4]

Application: WB    Species: mouse    Sample: RAW264.7 cells

Fig. 1| XIAOPI formula suppresses the polarization of M2 macrophages and CXCL1 expression.a The phenotype changes of RAW264.7 induced by 40 ng/ ml IL-4 and 40 ng/ml IL-13.
9). Protective effects of Da-cheng-qi decoction in rats with intracerebral hemorrhage. Phytomedicine, 2021 (PubMed: 34217968) [IF=7.9]

Application: WB    Species: Rat    Sample: glial cells

Fig. 5. DCQ and emodin reduced microglia activation after ICH. The results of the beam balance test (A) and elevated body swing test (B) were used to evaluate the neurological deficits of the Sham, SOL, EMO and DCQ rats (n = 15/group). Prussian blue staining was used to evaluate the iron deposition of rats (C, Bar = 50 μm). The intensities of prussian blue positive were analysed by ImageJ (D). Network showed the DEPs related to the lysosome and proteasome in DCQ/SOL (E). The DEPs involved in glial cell activation in CPu of DCQ rats were showed in (F). Prussian blue positive ameboid microglia were shown by immunohistochemical staining with Iba1 (a marker of microglia) (G, Bar = 50 μm). Levels of pro-inflammatory cytokines including IL-1β, IL-10, TNF-α and Arg1 in the CPu (H) and Hp (J) were measured by Western blotting (n = 6) and quantitatively analysed (I, K). Data were presented as means ± SEM. * p < 0.05, ** p < 0.01, *** p < 0.001 vs. Sham. # p < 0.05 vs. SOL. ▴ p < 0.05 vs. EMO.
10). Endometriosis derived exosomal miR-301a-3p mediates macrophage polarization via regulating PTEN-PI3K axis. BIOMEDICINE & PHARMACOTHERAPY, 2022 (PubMed: 35124383) [IF=7.5]
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