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CLDN11 encodes a member of the claudin family. Additionally we are shipping Claudin 11 Antibodies (69) and Claudin 11 Kits (33) and many more products for this protein.
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the expression of miR (show MLXIP Proteins)-99b was inversely correlated with CLDN11 levels . These findings suggest that a high level of miR (show MLXIP Proteins)-99b expression is an independent prognostic factor and correlates with poor survival of patients with Hepatocellular carcinoma (HCC (show FAM126A Proteins))
CLDN11 is an epigenetic biomarker for malignancy in dysplastic nevus and melanoma.
these data suggest that cancer cells may induce CLDN11 overexpression and subsequent collective migration of peritumoral CAFs (show TBX1 Proteins) via TGF-beta (show TGFB1 Proteins) secretion.
The expression of claudin-11 was up regulated in gastric cancer tissue.
The spatial organization of claudin-11 and connexin-43 (show GJA1 Proteins) is altered in men with primary seminiferous tubule failure.
disorganization of claudin-11 expression in Sertoli cells might be one of the factors involved in the impairment of spermatogenesis.
Treatment with 3-deazaneplanocin A, an inhibitor of H3K27 methyltransferase, attenuated CLDN11 induction by serum stimulation in parallel with sustained miR (show MLXIP Proteins)-1275 expression
claudin-11 may have a role in preventing cancer progression and may serve as a therapeutic target in reducing metastasis
late spermatogenic wave may negatively regulate claudin-11 gene activation and the subcellular localization of claudin-11 in Sertoli cells, thus altering the blood testis barrier in the human testis
hypermethylation of CLDN11, leading to downregulated expression, contributes to gastric carcinogenesis by increasing cellular motility and invasiveness
Results show that the primary function of claudin-11 is to provide a barrier that impedes the diffusion of material through the intramyelinic compartment
The present study provides the first evidence that DPT (show DPT Proteins) may be a novel effector of cadmium chloride, highlighting the significant role of DPT (show DPT Proteins) in the regulation of claudin-11 expression
Local radiation-induced testicular oxidative stress can elevate the expression of claudin-11 in the testis tissue.
Peptide octamers to modify the course of relapsing experimental autoimmune encephalomyelitis in SJL mice immunized with an oliogodendrocyte-specific protein peptide (OSP 55-71).
Spermatogenesis in all founder mice harboring two copies of the endogenous Cldn11 gene was normal. The promoter/enhancer of the transgene, upstream of exon 1 of the Cldn11 gene, is sufficient to rescue azoospermia in Cldn11-null mice.
we identified Cldn1 (show CLDN1 Proteins), Cldn2 (show CLDN2 Proteins) and Cldn11 as genes that discriminate between diverse types of M2 macrophages
Cldn11(-/-) Sertoli cells exhibit a unique phenotype whereby loss of tight junction integrity results in loss of the epithelial phenotype.
claudin-11 has a role in forming tight junctions in stria vascularis required for hearing through generation of endocochlear potential
These data demonstrate that OSP/claudin-11 and PLP (show C3 Proteins) have essential structural functions in maintaining normal compact myelin and there is redundancy in their functions.
K(V)3.1 K(+) current accounts for significant component of total K(+) current in oligodendrocyte lineage and, in association with OSP/claudin-11, plays significant role in OPC proliferation and migration and myelination of axons.
This gene encodes a member of the claudin family. Claudins are integral membrane proteins and components of tight junction strands. Tight junction strands serve as a physical barrier to prevent solutes and water from passing freely through the paracellular space between epithelial or endothelial cell sheets, and also play critical roles in maintaining cell polarity and signal transductions. The protein encoded by this gene is a major component of central nervous system (CNS) myelin and plays an important role in regulating proliferation and migration of oligodendrocytes. Mouse studies showed that the gene deficiency results in deafness and loss of the Sertoli cell epithelial phenotype in the testis. This protein is a tight junction protein at the human blood-testis barrier (BTB), and the BTB disruption is related to a dysfunction of this gene. Alternatively spliced transcript variants encoding different isoforms have been identified.
, claudin 11 (oligodendrocyte transmembrane protein)
, oligodendrocyte transmembrane protein
, oligodendrocyte-specific protein