anti-Nucleolar Protein 3 (Apoptosis Repressor with CARD Domain) (NOL3) 抗体

NOL3 encodes an anti-apoptotic protein that has been shown to down-regulate the enzyme activities of caspase 2, caspase 8 and tumor protein p53. 再加上,我们可以发Nucleolar Protein 3 (Apoptosis Repressor with CARD Domain) 蛋白 (12)和数多这个蛋白质的别的产品。

列出全部抗体 基因 基因ID UniProt
NOL3 8996 O60936
NOL3 78688 Q9D1X0
NOL3 85383 Q62881
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antibodies-online.cn销售最多的anti-Nucleolar Protein 3 (Apoptosis Repressor with CARD Domain) 抗体

Showing 10 out of 102 products:

产品编号 适用 宿主 标记 应用范围 图像 规格 交付 价格 详细
非结合性 WB WB Suggested Anti-NOL3 Antibody Titration:  0.2-1 ug/ml  ELISA Titer:  1:62500  Positive Control:  Human Muscle 100 μL 2至3个工作日
$289.00
详细
非结合性 ICC, IF, IHC, IHC (p), WB 100 μL 11至14个工作日
$537.17
详细
非结合性 WB Western blot analysis of Nop30 expression in MCF7 (A), HeLa (B), mouse brain (C), rat brain (D) whole cell lysates. 200 μL 13至14个工作日
$487.50
详细
非结合性 ELISA, IHC, IHC (p), WB Anti-NOL3 antibody IHC staining of human kidney, glomeruli. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval. Antibody  ABIN959355 concentration 10 ug/ml. 50 μL 11至14个工作日
$484.00
详细
非结合性 WB 100 μL 11至14个工作日
$551.83
详细
非结合性 IHC, IHC (p), IP, WB Anti-NOL3 antibody IHC staining of human prostate. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval. Antibody  ABIN1103290 dilution 5 ug/ml. Anti-NOL3 antibody IHC of human prostate. Immunohistochemistry of formalin-fixed, paraffin-embedded tissue after heat-induced antigen retrieval. Antibody dilution 5 ug/ml. 1 each 11至14个工作日
$639.83
详细
非结合性 ELISA, IF, IHC, WB 100 μL Available
$363.46
详细
非结合性 WB Anti-Apoptosis repressor with CARD antibody, Western blotting Lane 1: SMMC Cell Lysate Lane 2: A549 Cell Lysate Lane 3: U87 Cell Lysate Lane 4: HELA Cell Lysate Lane 5: MCF-7 Cell Lysate Lane 6: Rat Liver Tissue Lysate 100 μg 4至6个工作日
$240.00
详细
非结合性 EIA, WB   0.1 mg 4至8个工作日
$522.50
详细
非结合性 IHC, WB 0.1 mg 11至14个工作日
$551.83
详细

引用最多的anti-Nucleolar Protein 3 (Apoptosis Repressor with CARD Domain) 抗体

  1. Human Polyclonal NOL3 Primary Antibody for ELISA, WB - ABIN1002926 : Stoss, Schwaiger, Cooper, Stamm: Alternative splicing determines the intracellular localization of the novel nuclear protein Nop30 and its interaction with the splicing factor SRp30c. in The Journal of biological chemistry 1999 (PubMed)
    Show all 2 Pubmed References

  2. Human Polyclonal NOL3 Primary Antibody for WB - ABIN541153 : Koseki, Inohara, Chen, Núñez: ARC, an inhibitor of apoptosis expressed in skeletal muscle and heart that interacts selectively with caspases. in Proceedings of the National Academy of Sciences of the United States of America 1998 (PubMed)
    Show all 3 Pubmed References

  3. Human Polyclonal NOL3 Primary Antibody for WB - ABIN153055 : Mak, Mak, Ruvolo, Jacamo, Kornblau, Kantarjian, Andreeff, Carter: Apoptosis repressor with caspase recruitment domain modulates second mitochondrial-derived activator of caspases mimetic-induced cell death through BIRC2/MAP3K14 signalling in acute myeloid leukaemia. in British journal of haematology 2014 (PubMed)

  4. Human Polyclonal NOL3 Primary Antibody for ELISA, IHC - ABIN4281331 : Carter, Mak, Wang, Tao, Ruvolo, Mak, Mu, Burks, Andreeff: An ARC-Regulated IL1β/Cox-2/PGE2/β-Catenin/ARC Circuit Controls Leukemia-Microenvironment Interactions and Confers Drug Resistance in AML. in Cancer research 2019 (PubMed)

更多抗Nucleolar Protein 3 (Apoptosis Repressor with CARD Domain)的相互作用对抗体

Human Nucleolar Protein 3 (Apoptosis Repressor with CARD Domain) (NOL3) interaction partners

  1. Results show that in response to DNA damage, p53 total levels increase proportionally to the strength of the damage; however, p53 tetramers are formed at a constant rate under the control of ARC protein.

  2. role of apoptosis repressor with a CARD domain (ARC) in the therapeutic resistance of renal cell carcinoma

  3. a novel genetic primary myelofibrosis-like mouse model and identify a tumor suppressor role for NOL3 in the pathogenesis of myeloid malignancies.

  4. Increased ARC expression is associated with liver metastasis of colorectal cancer.

  5. RUNX3, miR-185 and ARC regulate the sensitivity of gastric cancer cells to chemotherapy.

  6. ARC is regulated via BIRC2/MAP3K14 signalling and its overexpression in AML or MSCs can function as a resistant factor to birinapant-induced leukaemia cell death.

  7. high expression of ARC plays an important role in the pathogenesis of nasopharyngeal carcinoma and leads to X-radiation and cisplatin resistance in nasopharyngeal carcinoma.

  8. ARC is a previously unrecognized inhibitor of apoptosis in beta-cells and that its protective effects are mediated through suppression of the ER stress response pathway.

  9. This study utilized unbiased, genome-wide approaches to identify a NOL3 mutation that likely causes Familial cortical myoclonus.

  10. HIF-1alpha directly bound to hypoxia-responsive element located at -419 to -414 of ARC gene, which is essential for HIF-1-induced expression.

  11. Data show that ARC promotes breast carcinogenesis by driving primary tumor growth, invasion, and metastasis as well as by promoting chemoresistance in invasive cells.

  12. ARC, previously unlinked to pulmonary hypertension, is a critical determinant of vascular remodeling in this syndrome.

  13. Results suggest that ARC expression levels are highly prognostic in AML and that ARC is a potential therapeutic target in AML.

  14. Ras induces ARC in epithelial cancers, and ARC plays a role in the oncogenic actions of Ras

  15. These results suggest that the antiapoptotic effect of apoptotic repressor with caspase recruitment domain is, in part, due to inhibition of voltage-gated potassium channels in cardiomyocytes.

  16. calcium binding mediates regulation of caspase 8 and cell death by ARC

  17. Unexpectedly, ARC was localized almost exclusively to the nuclei of cancer cells, which was unlike the cytoplasmic localization of ARC in non-cancer cells

  18. ARC was present in the cytoplasm and nuclei of epithelial cells in invasive ductal carcinoma

  19. is downregulated in human failing myocardium

  20. nuclear apoptosis repressor with caspase recruitment domain (ARC)is induced in cancer cells and negatively regulates p53

Mouse (Murine) Nucleolar Protein 3 (Apoptosis Repressor with CARD Domain) (NOL3) interaction partners

  1. our data revealed the pivotal role of ARC in myocardial necrosis and delineated the p53-ARC-CypD/mPTP central necrosis pathway, which can provide a potential therapeutic avenue for ischemia and oxidative stress-related cardiac diseases.

  2. Soleus of ARC-deficient mice exhibited lower total, as well as fiber type-specific cross sectional area in type I and IIA skeletal muscle fibers.

  3. Data suggest that reduced levels of apoptosis repressor with caspase recruitment domain protein (ARC) might correlate with neomycin-induced hair cells (HCs) loss.

  4. Although mice lacking Men1 developed insulinomas as expected, elimination of ARC in this context did not significantly alter tumor load. Cellular rates of proliferation and death in these tumors were also not perturbed in the absence of ARC.

  5. interaction of ARC with TNF receptor 1 Interferes with recruitment of RIP1, a critical mediator of TNFalpha-induced regulated necrosis.

  6. Arc deficiency in dystrophic muscle exacerbates disease pathogenesis due to a Bax-mediated sensitization of mitochondria-dependent death mechanisms

  7. ARC is a previously unrecognized inhibitor of apoptosis in beta-cells and that its protective effects are mediated through suppression of the ER stress response pathway.

  8. Data show that ARC promotes breast carcinogenesis by driving primary tumor growth, invasion, and metastasis as well as by promoting chemoresistance in invasive cells.

  9. ARC, previously unlinked to pulmonary hypertension, is a critical determinant of vascular remodeling in this syndrome.

  10. On biomechanical stress induced by aortic banding, ARC-deficient mice developed accelerated cardiomyopathy, which was characterized by reduced contractile function, cardiac enlargement, and myocardial fibrosis

  11. catalase, CK2, and ARC constitute an anti-hypertrophic pathway in the heart.

  12. endogenous nociceptin differentially modulates diet preference depending on macronutrient content and homeostatic state, independently of the motivating, rewarding or orosensory properties of food, but may involve metabolic or postingestive processes.

Nucleolar Protein 3 (Apoptosis Repressor with CARD Domain) (NOL3) 抗原简介

蛋白简介

This gene encodes an anti-apoptotic protein that has been shown to down-regulate the enzyme activities of caspase 2, caspase 8 and tumor protein p53. Multiple transcript variants encoding different isoforms have been found for this gene.

Gene names and symbols associated with NOL3

  • nucleolar protein 3 (NOL3) 抗体
  • nucleolar protein 3 (apoptosis repressor with CARD domain) (Nol3) 抗体
  • nucleolar protein 3 (Nol3) 抗体
  • nucleolar protein 3 (apoptosis repressor with CARD domain) (NOL3) 抗体
  • Arc 抗体
  • B430311C09Rik 抗体
  • FCM 抗体
  • MYC 抗体
  • MYP 抗体
  • NOP 抗体
  • Nop30 抗体

Protein level used designations for NOL3

muscle-enriched cytoplasmic protein , nucleolar protein 3 , nucleolar protein of 30 kDa , apoptosis repressor with CARD

GENE ID SPECIES
8996 Homo sapiens
78688 Mus musculus
85383 Rattus norvegicus
611249 Canis lupus familiaris
515777 Bos taurus
anti-Nucleolar Protein 3 (Apoptosis Repressor with CARD Domain) (NOL3) 抗体 精选生产商
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