anti-Selectin L (SELL) 抗体

SELL encodes a cell surface adhesion molecule that belongs to a family of adhesion/homing receptors. 再加上,我们可以发L-Selectin 试剂盒 (42)L-Selectin 蛋白 (31)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
SELL 6402 P14151
SELL 29259  
SELL 20343 P18337
How to order from antibodies-online
  • +1 877 302 8632
  • +1 888 205 9894 (toll-free)
  • 在线下订单
  • orders@antibodies-online.cn

antibodies-online.cn销售最多的anti-L-Selectin 抗体

Showing 10 out of 523 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
化学剂 非结合性 WB 100 μL 2至3个工作日
$289.00
详细
化学剂 大鼠 PE FACS Rat anti CD62L (L-Selectin, LECAM-1) MEL-14 50 μg 6至8个工作日
$258.50
详细
化学剂 非结合性 IP, IHC, WB Western blot analysis of L-Selectin expression in Jurkat cell lysate. 100 μg 2至3个工作日
$255.00
详细
化学剂 非结合性 ELISA, IHC (p), WB Immunohistochemistry (IHC) analysis of paraffin-embedded Rat Lung, antibody was diluted at 1:100. 100 μL Available
$363.46
详细
化学剂 非结合性 WB Western blot analysis of CD62L expression in A549 (A), NS-1 (B), PC12 (C) whole cell lysates. 200 μL 13至14个工作日
$487.50
详细
化学剂 大鼠 Biotin FACS Rat anti CD62L (L-Selectin, LECAM-1) MEL14 0.1 mg 6至8个工作日
$258.50
详细
化学剂 大鼠 FITC FACS Rat anti CD62L (L-Selectin, LECAM-1) MEL-14 0.1 mg 6至8个工作日
$269.50
详细
化学剂 非结合性 IHC (p), ELISA, WB Anti- CD62L Picoband antibody, IHC(P) IHC(P): Human Tonsil Tissue 100 μg 4至6个工作日
$280.00
详细
化学剂 大鼠 非结合性 Func, FACS, IHC (fro), IP Rat anti CD62L (L-Selectin, LECAM-1) MEL-14 0.25 mg 6至8个工作日
$368.50
详细
化学剂 非结合性 FACS, IF (p), IHC (p), WB Formalin-fixed and paraffin embedded mouse kidney tissue labeled with Rabbit Anti-L-Selectin/CD62L Polyclonal Antibody (ABIN736716), Unconjugated 1:200 followed by conjugation to the secondary antibody and DAB staining Formalin-fixed and paraffin embedded mouse kidney tissue labeled with Rabbit Anti-L-Selectin/CD62L Polyclonal Antibody (ABIN736716), Unconjugated 1:200 followed by conjugation to the secondary antibody and DAB staining 100 μL 3至7个工作日
$329.45
详细

引用最多的anti-L-Selectin 抗体

  1. Chemical Monoclonal L-Selectin Primary Antibody for BR, CyTox - ABIN2689360 : Reichert, Weissman, Butcher: Dual immunofluorescence studies of cortisone-induced thymic involution: evidence for a major cortical component to cortisone-resistant thymocytes. in Journal of immunology (Baltimore, Md. : 1950) 1986 (PubMed)
    Show all 19 Pubmed References

  2. Chemical Monoclonal L-Selectin Primary Antibody for BR, CyTox - ABIN1176858 : Jung, Gallatin, Weissman, Dailey: Down-regulation of homing receptors after T cell activation. in Journal of immunology (Baltimore, Md. : 1950) 1989 (PubMed)
    Show all 18 Pubmed References

  3. Chemical Monoclonal L-Selectin Primary Antibody for FACS - ABIN2689362 : Cerwenka, Carter, Reome, Swain, Dutton: In vivo persistence of CD8 polarized T cell subsets producing type 1 or type 2 cytokines. in Journal of immunology (Baltimore, Md. : 1950) 1998 (PubMed)
    Show all 18 Pubmed References

  4. Mouse (Murine) Monoclonal L-Selectin Primary Antibody for FACS, Func - ABIN457350 : Brawand, Cerottini, MacDonald: Hierarchal utilization of different T-cell receptor Vbeta gene segments in the CD8(+)-T-cell response to an immunodominant Moloney leukemia virus-encoded epitope in vivo. in Journal of virology 1999 (PubMed)
    Show all 9 Pubmed References

  5. Mouse (Murine) Monoclonal L-Selectin Primary Antibody for FACS, Func - ABIN457405 : Chen, Cui, Sempowski, Liu, Chao: Transfer of allogeneic CD62L- memory T cells without graft-versus-host disease. in Blood 2004 (PubMed)
    Show all 9 Pubmed References

  6. Mouse (Murine) Monoclonal L-Selectin Primary Antibody for FACS, Func - ABIN457432 : Chin, Miller, Graham, Parviz, Zacur, Patel, Duong, Bear: Bryostatin 1/ionomycin (B/I) ex vivo stimulation preferentially activates L-selectinlow tumor-sensitized lymphocytes. in International immunology 2004 (PubMed)
    Show all 8 Pubmed References

  7. Human Monoclonal L-Selectin Primary Antibody for FACS, Func - ABIN457338 : Abraham, Ahmed, Sabater, Lauredo, Botvinnikova, Bjercke, Hu, Revelle, Kogan, Scott, Dixon, Yeh, Beck: Selectin blockade prevents antigen-induced late bronchial responses and airway hyperresponsiveness in allergic sheep. in American journal of respiratory and critical care medicine 1999 (PubMed)
    Show all 7 Pubmed References

  8. Chemical Monoclonal L-Selectin Primary Antibody for CyTOF, ELISA (Capture) - ABIN4900543 : Chang, Eckert, Ali, Riazifar, Pone, Liu, Zhao: Facile supermolecular aptamer inhibitors of L-selectin. in PLoS ONE 2015 (PubMed)
    Show all 7 Pubmed References

  9. Human Monoclonal L-Selectin Primary Antibody for Func, IHC (f) - ABIN2749031 : Tu, Mao, Zheng, Liu, Chiu, Qin, Chan, Lam, Guan, Zhang, Guan, Yuen, Peiris, Lau: Cytotoxic T lymphocytes established by seasonal human influenza cross-react against 2009 pandemic H1N1 influenza virus. in Journal of virology 2010 (PubMed)
    Show all 6 Pubmed References

  10. Human Monoclonal L-Selectin Primary Antibody for FACS, Func - ABIN457418 : Killock, Parsons, Zarrouk, Ameer-Beg, Ridley, Haskard, Zvelebil, Ivetic: In Vitro and in Vivo Characterization of Molecular Interactions between Calmodulin, Ezrin/Radixin/Moesin, and L-selectin. in The Journal of biological chemistry 2009 (PubMed)
    Show all 6 Pubmed References

更多抗L-Selectin的相互作用对抗体

Human Selectin L (SELL) interaction partners

  1. L-selectin (CD62L) has been identified as an HIV-1 adhesion receptor on CD4+ T cells.

  2. PI3K is a signal linker between L-selectin and PSGL-1 in IL-18 transcriptional activation at the promoter level.

  3. SELL expression was not altered in systemic sclerosis.

  4. Dual regulation of CD62L by HIV-1 via enhanced expression by Vpr in contrast with cell-surface down-modulation by Nef and Vpu has been reported.

  5. The highest levels of sL- and sE-selectin were observed in colorectal patients with lymph node metastasis.

  6. Recombinant human IL33 inhibited trophoblast invasion and adhesion, and decreased adhesion and invasionassociated molecules such as integrin alpha4beta1 and CD62L.

  7. CD62L has merit for risk stratification in natalizumab treatment is associated with progressive multifocal leukoencephalopathy.

  8. sLe(x) expressed on human L-selectin is preferentially bound by E-selectin and, on ligation, initiates secretion of MRP8/14 that binds TLR4 to elicit the extension of beta2-integrin to an intermediate affinity state.

  9. Here, we further developed and applied this method to express and purify the entire extracellular region of CD62L. This resulted in excess of 20 mg/L yield of recombinant CD62L. In an attempt to understand the different expression levels among four similar CD62L constructs that differ primarily in signal sequences, we calculated the presence of potential RNA pseudoknots in their signal sequences

  10. identified CD62L as a marker of a distinct NKT subset endowed with high proliferative potential and have developed artificial antigen-presenting cells that generate CD62L-enriched NKTs for effective cancer immunotherapy

  11. The -642C>T and 725C>T SELL polymorphisms are protective factors against acute coronary syndrome. SELL gene expression was increased in ACS patients.

  12. CD62L downregulation due to unconstrained HIV-1 replication may have important consequences for T-cell circulation and function and for HIV-1 disease progression

  13. found a higher frequency of LIN1(-) CCR3(+) eosinophils, and decreased expression of CD23 and CD62L receptors in eosinophils of AD patients

  14. Indian patients with primary Sjogren's syndrome have higher salivary sL-selectin and IL-7 levels than healthy controls

  15. While total surface expression of CD11b and L-selectin on neutrophils was largely unaffected

  16. Data show that both mucin16 (MUC16) and podocalyxin (PODXL)-E-selectin-mediated interactions are mechanically stronger than like L-selectin interactions at the single-molecule level.

  17. These data confirm the expression of CD62L on urothelial carcinoma cells and suggest that CD62L may serve as biomarker to predict the presence of or risk for developing metastatic disease in patients with bladder cancer.

  18. freeze and thaw of murine and human Tregs is associated with reduced expression of L-selectin (CD62L), which was previously established to be an important factor that contributes to the in vivo protective effects of Tregs

  19. Modification of Levels of Adhesion Molecule Expression of Human Innate Immune Cells by Glycopolymers of Marine Bacteria

  20. Here we report that HIV-1 down-modulates CD62L in productively infected naive and memory resting CD4 T cells while suppressing Foxo1 activity and the expression of KLF2 mRNA.

Cow (Bovine) Selectin L (SELL) interaction partners

  1. Five single nucleotide polymorphisms (SNPs) from different exons in selectin SELP, two in selectin SELL and one in selectin SELE were taken forward to genotyping in 337 Holstein Friesian heifers using PCR-RFLP.

  2. gammadelta T cells, the main recirculating subset in both afferent and efferent lymph, have high levels of CD62L cell surface expression.

  3. demonstrate the existence of central memory T cells (Tcm) in cattle and suggest that CD62L may serve as a marker to monitor Tcm in infections and vaccine development studies in ruminant.

  4. determined the effects of Mycobacterium-induced proliferation and apoptosis on CD25, CD44, and CD62L expression on peripheral blood T-cell subsets from M. bovis-infected cattle

  5. intramammarily administered lipopolysaccharides seem to play an important role in modulating L-selectin and beta2 integrin expression on circulating bovine polymorphonuclear leukocytes

  6. results indicate that glucocorticoid-induced suppression of L-selectin is likely mediated by direct effects of glucocorticoid receptor activation on intracellular reservoirs of L-selectin mRNA and protein, predominantly in blood neutrophils.

Mouse (Murine) Selectin L (SELL) interaction partners

  1. These findings suggest that interactions between MAdCAM-1 and alpha4beta7 integrin and/or unsulfated sLeX and L-selectin may become a dominant mechanism for inflammatory cell recruitment in the absence of 6-sulfo sLeX and contribute to more severe colitis phenotypes seen in mice deficient in both GlcNAc6ST-1 and GlcNAc6ST-2.

  2. evidence that chronic inflammation may promote tumor growth via induction of CD62L expression by MDSCs that can facilitate their migration to tumor and lymph nodes and modulation of their suppressor activity.

  3. data suggest that Ly6C(+)CD62L(+) infected monocytes served as a Trojan horse across the cerebral endothelium to induce brain infection. Therefore, CD62L should be considered as not only a temporally elicited antigen but also a disease-relevant leukocyte marker during the development of neurologic melioidosis.

  4. Myeloid-derived suppressor cell-induced L-selectin loss occurs through a contact-dependent, post-transcriptional mechanism that is independent of the major L-selectin sheddase, ADAM17, but results in significant elevation of circulating L-selectin in tumor-bearing mice.

  5. CD8(+) T-cells mediate ischemia reperfusion injury in a fatty liver through L-selectin.

  6. L-selectin is transported constitutively by the AP-1 complex, leading to the formation of a trans-Golgi network reserve pool; phosphorylation of the L-selectin tail blocks AP-1-dependent retrograde transport of L-selectin

  7. freeze and thaw of murine and human Tregs is associated with reduced expression of L-selectin (CD62L), which was previously established to be an important factor that contributes to the in vivo protective effects of Tregs

  8. endothelial colony-forming cells interact with activated neutrophils via PSGL-1 and L-selectin

  9. These data indicate that L-selectin plays a major role in the development of C protein induced polymyositis, whereas ICAM-1 plays a lesser role, if any.

  10. Data suggest that modulation of P- and L-selectins may constitute a promising therapeutic approach.

  11. These results put into question the utility of CD62L as a predictive biomarker for the efficacy of ex vivo-expanded T cells after ACT in lymphopenic conditions.

  12. The PSGL-1-L-selectin complex-induced signaling effects on neutrophil slow rolling and recruitment in vivo demonstrate the functional importance of this pathway.

  13. L-selectin-dependent signalling - exploring the different signals that potentially arise from distinct phases of the multi-step adhesion cascade and the contribution of known binding partners of L-selectin in this respon

  14. CD62L marks a mature natural killer (NK) cell subset by affecting the magnitude of the local NK cell response to adenovirus infection in the liver.

  15. Data indicate that naive lung CD4 cells supply the draining lymph nodes through a CD62L-independent, CCR7-dependent pathway.

  16. Signaling induced by ligation of L-selectin using mAb or endothelial cell-expressed ligand significantly enhanced the chemotaxis of murine T cells and B cells to SLC but not to other homeostatic chemokines.

  17. Pretreatment of cardiac mesoangioblasts with SDF-1 or transient expression of L-selectin induced a two- to three-fold increase in their transmigration and homing to the damaged heart.

  18. Hematopoietic lineage cells with Sca-1(high) expression and CD62L(neg/low) expression are characterized as multipotent progenitor cells, based on transient engraftment.

  19. the binding of L-selectin to its vascular and extravascular ligands is differentially regulated by pH.

  20. CD4 T cell co-stimulation with ICOS promotes the down-regulation of CCR7 and CD62L after activation, leading to a reduced return of activated CD4 T cells to the lymph nodes and a more efficient entry into the lungs.

L-Selectin (SELL) 抗原简介

蛋白简介

This gene encodes a cell surface adhesion molecule that belongs to a family of adhesion/homing receptors. The encoded protein contains a C-type lectin-like domain, a calcium-binding epidermal growth factor-like domain, and two short complement-like repeats. The gene product is required for binding and subsequent rolling of leucocytes on endothelial cells, facilitating their migration into secondary lymphoid organs and inflammation sites. Single-nucleotide polymorphisms in this gene have been associated with various diseases including immunoglobulin A nephropathy. Alternatively spliced transcript variants have been found for this gene.

Gene names and symbols associated with anti-Selectin L (SELL) 抗体

  • selectin L (SELL) 抗体
  • selectin L (Sell) 抗体
  • selectin, lymphocyte (Sell) 抗体
  • A.11 抗体
  • AI528707 抗体
  • CD62L 抗体
  • L-selectin 抗体
  • LAM1 抗体
  • LECAM-1 抗体
  • LECAM1 抗体
  • LEU8 抗体
  • Lnhr 抗体
  • LSEL 抗体
  • Ly-22 抗体
  • Ly-m22 抗体
  • Lyam-1 抗体
  • Lyam1 抗体
  • PLNHR 抗体
  • SELE 抗体
  • TQ1 抗体

Protein level used designations for anti-Selectin L (SELL) 抗体

CD62 antigen-like family member L , L-selectin , gp90-MEL , leukocyte surface antigen Leu-8 , leukocyte-endothelial cell adhesion molecule 1 , lymph node homing receptor , lymphocyte adhesion molecule 1 , pln homing receptor , LAM-1 , LECAM1 , leukocyte adhesion molecule 1 , ly-22 , lymphocyte antigen 22 , lymphocyte surface MEL-14 antigen , selectin, lymphocyte , selectin L (lymphocyte adhesion molecule 1) , selectin E (endothelial adhesion molecule 1)

GENE ID SPECIES
6402 Homo sapiens
29259 Rattus norvegicus
100009204 Oryctolagus cuniculus
100716722 Cavia porcellus
100127147 Sus scrofa
281485 Bos taurus
480080 Canis lupus familiaris
101102077 Ovis aries
701419 Macaca mulatta
450191 Pan troglodytes
20343 Mus musculus
anti-L-Selectin (SELL) 抗体 精选生产商
您还需要查找其他产品吗?