F227A抗体应用：WB 1:500-2000

F25DE抗体应用：WB 1:500-2000

F91A2抗体应用：WB 1:500-2000

DLG1抗体应用：WB 1:500-2000 ELISA 1:5000-20000discs large MAGUK scaffold protein 1(DLG1) Homo sapiens This gene encodes a multi-domain scaffolding protein that is required for normal development. This protein may have a role in septate junction formation, signal transduction, cell proliferation, synaptogenesis and lymphocyte activation. Several alternatively spliced transcript variants encoding different isoforms have been described for this gene, but the full-length nature of some of the variants is not known. [provided by RefSeq, Feb 2011],

DLG3抗体应用：WB 1:500-2000 ELISA 1:5000-20000discs large MAGUK scaffold protein 3(DLG3) Homo sapiens This gene encodes a member of the membrane-associated guanylate kinase protein family. The encoded protein may play a role in clustering of NMDA receptors at excitatory synapses. It may also negatively regulate cell proliferation through interaction with the C-terminal region of the adenomatosis polyposis coli tumor suppressor protein. Mutations in this gene have been associated with X-linked mental retardation. Alternatively spliced transcript variants have been described. [provided by RefSeq, Oct 2009],

DLGP4抗体应用：WB 1:500-2000 The product of this gene is a membrane-associated guanylate kinase found at the postsynaptic density in neuronal cells. It is a signaling molecule that can interact with potassium channels and receptors, as well as other signaling molecules. The protein encoded by this gene can interact with PSD-95 through its guanylate kinase domain and may be involved in clustering PSD-95 in the postsynaptic density region. The encoded protein is one of at least four similar proteins that have been found. Alternatively spliced transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Jul 2008],

DLL1抗体应用：WB 1:500-2000 ELISA 1:5000-20000delta like canonical Notch ligand 1(DLL1) Homo sapiens DLL1 is a human homolog of the Notch Delta ligand and is a member of the delta/serrate/jagged family. It plays a role in mediating cell fate decisions during hematopoiesis. It may play a role in cell-to-cell communication. [provided by RefSeq, Jul 2008],

DLL3抗体应用：WB 1:500-2000 ELISA 1:5000-20000delta like canonical Notch ligand 3(DLL3) Homo sapiens This gene encodes a member of the delta protein ligand family. This family functions as Notch ligands that are characterized by a DSL domain, EGF repeats, and a transmembrane domain. Mutations in this gene cause autosomal recessive spondylocostal dysostosis 1. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq, Jul 2008],

DLL4抗体应用：WB 1:500-2000 ELISA 1:5000-20000delta like canonical Notch ligand 4(DLL4) Homo sapiens This gene is a homolog of the Drosophila delta gene. The delta gene family encodes Notch ligands that are characterized by a DSL domain, EGF repeats, and a transmembrane domain. [provided by RefSeq, Jul 2008],

DLRB1抗体应用：WB 1:500-2000 ELISA 1:5000-20000dynein light chain roadblock-type 1(DYNLRB1) Homo sapiens This gene is a member of the roadblock dynein light chain family. The encoded cytoplasmic protein is capable of binding intermediate chain proteins, interacts with transforming growth factor-beta, and has been implicated in the regulation of actin modulating proteins. Upregulation of this gene has been associated with hepatocellular carcinomas, suggesting that this gene may be involved in tumor progression. Alternative splicing results in multiple transcript variants. Pseudogenes of this gene have been defined on chromosomes 12 and 18. [provided by RefSeq, Aug 2013],