anti-LIM and Senescent Cell Antigen-Like Domains 1 (LIMS1) 抗体

The protein encoded by LIMS1 is an adaptor protein which contains five LIM domains, or double zinc fingers. 再加上,我们可以发LIM and Senescent Cell Antigen-Like Domains 1 蛋白 (5)LIM and Senescent Cell Antigen-Like Domains 1 试剂盒 (1)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
LIMS1 3987 P48059
LIMS1 499443  
LIMS1 110829 Q99JW4
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antibodies-online.cn销售最多的anti-LIM and Senescent Cell Antigen-Like Domains 1 抗体

Showing 10 out of 70 products:

产品编号 适用 宿主 标记 应用范围 图像 规格 供应商 交付 价格 详细
Cow 非结合性 WB WB Suggested Anti-LIMS1 Antibody Titration: 1.0 ug/ml Positive Control: U937 Whole Cell 100 μL Log in to see 2至3个工作日
$289.00
详细
Cow 非结合性 WB Host: RabbitTarget Name: LIMS1Antibody Dilution: 1.0ug/mlSample Tissue: MCF7 cell lysate 100 μL Log in to see 2至3个工作日
$289.00
详细
小鼠 非结合性 ELISA, FACS, ICC, WB Red: Control Antigen (100ng);Purple: Antigen (10ng);Green: Antigen (50ng);Blue: Antigen (100ng); Dilution: 1/10000 Figure 1: Western blot analysis using PINCH mAb against human PINCH (AA: 87-249) recombinant protein. (Expected MW is 44.2 kDa)  Dilution: 1/500 - 1/2000 100 μL Log in to see 8至11个工作日
$577.50
详细
小鸡 小鼠 非结合性 IF, WB Western blot analysis of PINCH on K-562 lysate. Lane 1: 1:1000, lane 2: 1:2000, lane 3: 1:4000 dilution of anti-PINCH antibody. 150 μg Log in to see 15至18个工作日
$319.62
详细
小鼠 非结合性 ELISA, FACS, ICC, IF, WB Immunocytochemistry/Immunofluorescence: PINCH1/LIMS1 Antibody (5G7) [NBP2-37581] - Immunofluorescence analysis of HepG2 cells using PINCH mouse mAb (green). Blue: DRAQ5 fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin. Western Blot: PINCH1/LIMS1 Antibody (5G7) [NBP2-37581] - Western blot analysis using PINCH mouse mAb against A549 (1), Jurkat (2), and Hela (3) cell lysate. 0.1 mL Log in to see 7至9个工作日
$559.35
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小鼠 非结合性 ELISA, FACS 100 μL Log in to see 11至14个工作日
$551.83
详细
小鼠 非结合性 ELISA, FACS, IF/ICC, WB 100 μL Log in to see 11至16个工作日
$426.40
详细
小鼠 非结合性 ELISA, FACS, IF, WB Western blot analysis using LIMS1 monoclonal antobody, clone 5G7  against A-549 (1), Jurkat (2), and HeLa (3) cell lysate. Immunofluorescence analysis of HepG2 cells using LIMS1 monoclonal antobody, clone 5G7  (green). Blue: DRAQ5 fluorescent DNA dye. Red: Actin filaments have been labeled with Alexa Fluor-555 phalloidin. 100 μL Log in to see 11至12个工作日
$452.00
详细
非结合性 WB LIMS3/LIMS3L Antibody (Center) western blot analysis in 293 cell line lysates (35ug/lane).This demonstrates the LIMS3/LIMS3L antibody detected the LIMS3/LIMS3L protein (arrow). 400 μL Log in to see 10至11个工作日
$385.00
详细
非结合性 ICC, IHC, WB Western Blot; Sample: Human Lung lysate; Primary Ab: 1µg/ml Rabbit Anti-Human LIMS1 Antibody Second Ab: 0.2µg/mL HRP-Linked Caprine Anti-Rabbit IgG Polyclonal Antibody (Catalog: SAA544Rb19) 100 μg Log in to see 13至16个工作日
$384.00
详细

引用最多的anti-LIM and Senescent Cell Antigen-Like Domains 1 抗体

  1. Chicken Monoclonal LIMS1 Primary Antibody for IF, WB - ABIN968921 : Campana, Myers, Rearden: Identification of PINCH in Schwann cells and DRG neurons: shuttling and signaling after nerve injury. in Glia 2003 (PubMed)
    Show all 3 Pubmed References

  2. Human Monoclonal LIMS1 Primary Antibody for FACS, IF - ABIN966832 : Yang, Wang, Hawkins, Chen, Vaynberg, Mao, Tu, Zuo, Wang, Wang, Wu, Tjandra, Qin: Structural basis of focal adhesion localization of LIM-only adaptor PINCH by integrin-linked kinase. in The Journal of biological chemistry 2009 (PubMed)
    Show all 2 Pubmed References

  3. Human Monoclonal LIMS1 Primary Antibody for ICC, FACS - ABIN969354 : Chiswell, Zhang, Murphy, Boggon, Calderwood: The structural basis of integrin-linked kinase-PINCH interactions. in Proceedings of the National Academy of Sciences of the United States of America 2008 (PubMed)
    Show all 2 Pubmed References

更多抗LIM and Senescent Cell Antigen-Like Domains 1的相互作用对抗体

Human LIM and Senescent Cell Antigen-Like Domains 1 (LIMS1) interaction partners

  1. High LIMS1 expression is associated with Neuroblastoma.

  2. focal adhesion signaling to actin cytoskeleton is implicated in human laryngeal carcinogenesis and PINCH1 has prognostic significance in the disease.

  3. that PINCH-1 may be playing an important role in etiopathogenesis of both subtypes breast cancer

  4. Mammalian cells have two functional PINCH proteins, PINCH1 and PINCH2. PINCH not only binds to Nck2 and engages in the signaling of growth factor receptors, but also forms a ternary complex with ILK and parvin (IPP complex).

  5. our data suggest an essential role of PINCH1, ILK and ILKAP for the radioresistance of p53-wildtype glioblastoma multiforme cells

  6. Data suggest that PINCH1 and Nck2 critically participate in the regulation of cellular radiosensitivity and EGFR function and downstream signaling in a cellular model of human squamous cell carcinoma.

  7. Downregulation of PINCH1 is associated with metastatic breast cancer.

  8. changes in CSF levels of PINCH appear to correlate with changes in blood CD4 count and with changes in CSF hyperphosphorylated Tau levels

  9. two novel genes, galectin 9 and PINCH, were expressed at much higher levels in cancerous lesions than in normal tissues in all the patients with clear-cell carcinoma who were examined

  10. PINCH predicts survival in rectal cancer patients with RT, but not in patients without RT. The expression of PINCH may be regulated by radiation and by environmental factors surrounding the cells.

  11. PINCH is increased and binds to hp-Tau. These studies address a new mechanism by which AD and HIV may intersect and identify PINCH as a contributing factor to the accumulation of hyperphosphorylated Tau.

  12. Pinch-1 mRNA and protein were significantly up-regulated in acute lymphoblastic leukemia and acute myeloid leukemia bone marrow stromal cells compared to normal bone marrow stromal cells (p<0.01).

  13. PINCH protein might play an important role in the tumourigenesis and metastasis of gastric adenocarcinoma.

  14. PINCH mRNA overexpression in colorectal carcinomas is correlated with VEGF and FAS mRNA expression

  15. PINCH may function as a neuron-specific host-mediated response to challenge by HIV-related factors in the CNS.

  16. PINCH1 can shuttle into the nucleus from cytoplasm in podocytes, wherein it interacts with WT1 and suppresses podocyte-specific gene expression.

  17. Review provides an overview of the current knowledge of the molecular interactions of PINCH with other components of focal adhesions and discusses its potential implication for human heart disease.

  18. data reveal how specific domains of PINCH-1 direct two independent pathways: one utilizing ILK to allow cell attachment, and the other recruiting Rsu-1 to activate Rac1 in order to promote cell spreading

  19. PINCH staining at the tumour invasive margin was related to survival in poorly differentiated tumours but not in better differentiated tumours, indicating that the impact of PINCH on prognosis was dependent on differentiation status.

  20. Data suggest that the adapter protein PINCH1 critically participates in the regulation of the cellular radiosensitivity of normal and malignant cells similarly under adhesion and suspension conditions.

Mouse (Murine) LIM and Senescent Cell Antigen-Like Domains 1 (LIMS1) interaction partners

  1. findings suggest that PINCH-1 regulates integrin-mediated adhesion of keratinocytes through the interactions with ILK as well as EPLIN.

  2. Rsu-1 expression is dramatically decreased in PINCH double knockout mouse livers.

  3. PINCH is increased and binds to hp-Tau. These studies address a new mechanism by which AD and HIV may intersect and identify PINCH as a contributing factor to the accumulation of hyperphosphorylated Tau.

  4. PINCH-1 inhibits JNK-mediated apoptosis by stabilising the PINCH-1 binding protein RSU-1 and promotes Bcl-2-dependent pro-survival signalling downstream of integrins.

  5. Data suggest that the adapter protein PINCH1 critically participates in the regulation of the cellular radiosensitivity of normal and malignant cells similarly under adhesion and suspension conditions.

  6. PINCH1 plays an essential role in early murine embryonic development but is dispensable in ventricular cardiomyocytes.

  7. These results provide important evidence for a crucial role of the PINCH-1-ILK-alpha-parvin complex in the control of podocyte adhesion, morphology, and survival.

  8. LIM 5 domain of PINCH1 interacts with Rsu-1 in mammalian cells and functions, in part, by altering cell adhesion.

  9. The PINCH1 is composed of 5 LIM domains, binds ILK and locates to integrin-mediated adhesion sites, and PINCH1 is for integrin function, actin organization, cell-cell adhesion and endodermal cell survival during the implanting of mouse embryos.

  10. PICH1, Ilk and alpha-parvin form a complex to costameres in neonatal mouse ventricular myocytes. This complex is stimulated by fibronectins and phenylephrine, and by both by drug synergism, to regulate cardiac myocyte hypertrophy.

  11. LIM1 domain only of either PINCH1 or PINCH2 can prevent ILK degradation despite their failure to localize to focal adhesions.

  12. Transactivation studies and chromatin immunoprecipitation implicate Lims1 as a direct target of NF-E2 regulation

  13. Pinch1 plays an essential role in neural crest development, in part through transforming growth factor-beta signaling.

  14. mechanical stretch prevented vascular smooth muscle from apoptosis via a mechanism that involves alphaVbeta3 integrin expression, stabilization of PINCH-1, and remodeling of the cytoskeleton.

  15. Results describe the roles of the ILK-PINCH-parvin triad proteins in the maturation of focal adhesions.

  16. Absence of either PINCH1 or PINCH2 in myocardium leads to exacerbated cardiac injury and deterioration in cardiac function after myocardial infarction.

LIM and Senescent Cell Antigen-Like Domains 1 (LIMS1) 抗原简介

蛋白简介

The protein encoded by this gene is an adaptor protein which contains five LIM domains, or double zinc fingers. The protein is likely involved in integrin signaling through its LIM domain-mediated interaction with integrin-linked kinase, found in focal adhesion plaques. It is also thought to act as a bridge linking integrin-linked kinase to NCK adaptor protein 2, which is involved in growth factor receptor kinase signaling pathways. Its localization to the periphery of spreading cells also suggests that this protein may play a role in integrin-mediated cell adhesion or spreading. Several transcript variants encoding different isoforms have been found for this gene.

Gene names and symbols associated with LIMS1

  • LIM zinc finger domain containing 1 (LIMS1) 抗体
  • LIM zinc finger domain containing 1 (Lims1) 抗体
  • LIM and senescent cell antigen-like domains 1 (Lims1) 抗体
  • 2310016J22Rik 抗体
  • 4921524A02Rik 抗体
  • AI507642 抗体
  • AU021743 抗体
  • AW551584 抗体
  • C430041B13Rik 抗体
  • Lims1l 抗体
  • LIMS3 抗体
  • LIMS3L 抗体
  • PINCH 抗体
  • PINCH-1 抗体
  • Pinch1 抗体
  • RGD1560732 抗体

Protein level used designations for LIMS1

LIM and senescent cell antigen-like-containing domain protein 1 , particularly interesting new Cys-His protein 1 , renal carcinoma antigen NY-REN-48

GENE ID SPECIES
3987 Homo sapiens
499443 Rattus norvegicus
414880 Gallus gallus
474540 Canis lupus familiaris
100511559 Sus scrofa
540281 Bos taurus
110829 Mus musculus
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