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The protein encoded by EPB41, together with spectrin and actin, constitute the red cell membrane cytoskeletal network. Zusätzlich bieten wir Ihnen Erythrocyte Membrane Protein Band 4.1 (Elliptocytosis 1, RH-Linked) Antikörper (63) und Erythrocyte Membrane Protein Band 4.1 (Elliptocytosis 1, RH-Linked) Proteine (8) und viele weitere Produktgruppen zu diesem Protein an.
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Our study shows alternative polyadenylation to be an additional mechanism for the generation of 4.1 protein diversity in the already complex EPB41-related genes. Understanding the diversity of EPB41 RNA processing is essential for a full appreciation of the many 4.1 proteins expressed in normal and pathological tissues.
identification of EPB41 as a hepatocellular carcinoma susceptibility gene in vitro and in vivo; consistent with this notion, EPB41 expression is significantly decreased in HCC (zeige FAM126A ELISA Kits) tissue specimens, especially in portal vein metastasis or intrahepatic metastasis, compared to normal tissues
The 4.1R, 4.1N (zeige EPB41L1 ELISA Kits) and 4.1B (zeige EPB41L3 ELISA Kits) are all expressed at the lateral membrane as well as cytoplasm of epithelial cells, suggesting a potentially redundant role of these proteins.
Calcium mediates the conformation-based 4.1R FERM domain binding to membrane proteins by calmodulin (zeige CALM1 ELISA Kits).
Results suggest a previously unidentified role for the scaffolding protein 4.1R in locally controlling CLASP2 (zeige CLASP2 ELISA Kits) behavior, CLASP2 (zeige CLASP2 ELISA Kits) cortical platform turnover and GSK3 (zeige GSK3b ELISA Kits) activity, enabling correct MT organization and dynamics essential for cell polarity.
We conclude that PIP2 may play an important role as a modulator of apo (zeige C9orf3 ELISA Kits)-CaM (zeige CALM1 ELISA Kits) binding to 4.1R(80) throughout evolution.
Plasmodium falciparum PF3D7_0402000 was identified as a new binding partner for the major erythrocyte cytoskeletal protein (zeige ACTN1 ELISA Kits), 4.1R.
a novel gene region, EPB41, which may be associated with smoking cessation, along with gene regions in CNR1 (zeige CNR1 ELISA Kits) that may be targeted to further elucidate the etiology of gender differences in smoking behaviors.
4.1R regulates NHE1 (zeige SLC9A1 ELISA Kits) activity through a direct protein-protein interaction that can be modulated by intracellular pH and Na(+) and Ca(2 (zeige CA2 ELISA Kits)+) concentrations.
Further studies involving siRNA-mediated knockdowns of spectrin, adducin, or p4.1 revealed that those proteins are needed for efficient docking of enterohaemorrhagic Escherichia coli to host cells.
Data hypothesize that protein 4.1 (4.1R) could function as a linker protein (zeige LAT ELISA Kits) between cytokeratin (zeige KRT1 ELISA Kits) and the actin-based cytoskeleton.
4.1G interacts with a subset of CNG (zeige CNGA1 ELISA Kits) channels and implicate this protein-protein interaction in organizing the spatial arrangement of CNG (zeige CNGA1 ELISA Kits) channels in the plasma membrane of retinal outer segments.
Band 4.1 protein is found in a retinal cDNA library screened for proteins interacting with the intracellular C-terminus of the metabotropic glutamate (zeige GRIN2A ELISA Kits) receptor isoform 8a (mGluR8a).
This suggests that 4.1R may influence myogenesis by preventing VHL (zeige VHL ELISA Kits)-mediated myogenin (zeige MYOG ELISA Kits) degradation.
The proportion of 4.1R-positive cells was significantly higher in the HF group than in the controls, which was confirmed by the positive mRNA expression of 4.1R. 4.1R localized mostly to the plasma membrane of myocardial cells and was upregulated with the progression of HF. This suggests that 4.1R may be associated with HF progression.
suggest that 4.1R can prevent pathogenic autoimmunity in MS/EAE progression by suppressing the CD4 (zeige CD4 ELISA Kits)(+) T cell activation
Loss of 4.1/NuMA (zeige NUMA1 ELISA Kits) interaction results in spindle orientation defects and inhibition of Cdk1 (zeige CDK1 ELISA Kits) causes increase in cortical NuMA (zeige NUMA1 ELISA Kits) localization
a functional role for 4.1R in small intestinal calcium absorption through regulation of membrane expression of PMCA1b (zeige ATP2B1 ELISA Kits).
At the intercalated disc 4.1R does not colocalise with the adherens junction protein, beta-catenin (zeige CTNNB1 ELISA Kits), but does overlap with the other plasma membrane signalling proteins, the Na/K-ATPase (zeige ATP1A1 ELISA Kits) and the Na/Ca exchanger NCX1 (zeige SLC8A1 ELISA Kits).
Cell adhesion and signaling pathways regulated by alphavbeta8 integrin and Band 4.1B (zeige EPB41L3 ELISA Kits) are essential for normal formation and function of the heart during embryogenesis.
A conserved exonic splicing silencer element (CE(16)) in protein 4.1R exon 16 (E16 (zeige SLC7A5 ELISA Kits)) interacts with hnRNP A/B (zeige HNRNPAB ELISA Kits) proteins & plays a role in repression of E16 (zeige SLC7A5 ELISA Kits) splicing during early erythropoiesis
We speculate that over the repetitive cycles of heart muscle contraction and relaxation, 4.1R is likely to locate, support, and coordinate functioning of key membrane-bound macromolecular assemblies.[Epb41]
These results suggest that erythroid protein 4.1 plays a major role in volume regulation and physiologically downregulates Na/H exchange in mouse erythrocytes.
The protein encoded by this gene, together with spectrin and actin, constitute the red cell membrane cytoskeletal network. This complex plays a critical role in erythrocyte shape and deformability. Mutations in this gene are associated with type 1 elliptocytosis (EL1). Alternatively spliced transcript variants encoding different isoforms have been described for this gene.
erythrocyte membrane protein band 4.1 (elliptocytosis 1, RH-linked)
, protein 4.1R
, cytoskeletal protein 4.1
, protein 4.1
, protein 4.1-like
, band 4.1
, erythrocyte surface protein band 4.1
, erythroid membrane skeletal protein 4.1
, erythroid protein 4.1