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Dystroglycan 1 (Dystrophin-Associated Glycoprotein 1) (DAG1) ELISA Kits

Dystroglycan is a laminin binding component of the dystrophin-glycoprotein complex which provides a linkage between the subsarcolemmal cytoskeleton and the extracellular matrix. Additionally we are shipping Dystroglycan 1 (Dystrophin-Associated Glycoprotein 1) Antibodies (1) and many more products for this protein.

list all ELISA KIts Gene Name GeneID UniProt
Anti-Rat DAG1 DAG1 114489  
DAG1 13138 Q62165
DAG1 1605 Q14118
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Top Dystroglycan 1 (Dystrophin-Associated Glycoprotein 1) ELISA Kits at antibodies-online.com

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Catalog No. Reactivity Sensitivity Range Quantity Supplier Delivery Price Details
Human 31.25 pg/ml 125-8000 pg/mL 96 Tests Log in to see 11 to 13 Days
$910.56
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Pig
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$770.00
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Chicken
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$770.00
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Monkey
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Rabbit
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Guinea Pig
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Mouse 0.054 ng/mL 0.156-10 ng/mL 96 Tests Log in to see 5 to 9 Days
$1,046.42
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More ELISA Kits for Dystroglycan 1 (Dystrophin-Associated Glycoprotein 1) Interaction Partners

Fruit Fly (Drosophila melanogaster) Dystroglycan 1 (Dystrophin-Associated Glycoprotein 1) (DAG1) interaction partners

  1. in Drosophila the microRNA complex miR (show MYLIP ELISA Kits)-310s acts as an executive mechanism to buffer levels of the muscular dystrophy-associated extracellular matrix receptor dystroglycan via its alternative 3'-UTR (show UTS2R ELISA Kits)

  2. photoreceptor(R) cell differentiation defects appear at the same stage in a deficiency line Df(2R)Dg(248) that affects Dystroglycan (DG) and the neighboring mitochondrial ribosomal gene, mRpL34 (show MRPL34 ELISA Kits); findings discussed in view of recent work implicating DG as a regulator of cell metabolism and its genetic interaction with mRpL34 (show MRPL34 ELISA Kits)

  3. Nrk (show NRK ELISA Kits), mbl, capt and Cam (show CALM ELISA Kits) genetically interact with dystrophin (show DMD ELISA Kits) and/or dystroglycan in the process of axon path-finding in the eye.

  4. differential splicing of Dystroglycan is developmentally regulated and tissue-specific

  5. only dystroglycan, but not dystrophin (show DMD ELISA Kits) deficiency causes myodegeneration induced by energetic stress suggesting that dystroglycan might be a component of the low-energy pathway and act as a transducer of energetic stress in normal and dystrophic muscles

  6. the primary function of Dystroglycan in oogenesis is to organize cellular polarity

  7. Dystroglycan links EGF receptor (show EGFR ELISA Kits)-induced repression of the anterior follicle cell fate and anterior-posterior polarity formation in the oocyte

  8. The interaction of perlecan (show HSPG2 ELISA Kits) and dystroglycan at the basal side of the epithelium promotes basal membrane differentiation and is required for maintenance of cell polarity in the follicle-cell epithelium.

  9. The synaptic role of Dystroglycan (Dg) in Drosophila, is studied.

  10. Results suggest that Perlecan signaling through Dystroglycan may determine where Myosin II can be activated by AMPK, thereby providing the basal polarity cue for the low-energy epithelial polarity pathway.

Caenorhabditis elegans (C. elegans) Dystroglycan 1 (Dystrophin-Associated Glycoprotein 1) (DAG1) interaction partners

  1. We find that the dystroglycan ortholog DGN-1 mediates the fidelity of follower lumbar commissure axon extension along the pioneer axon route

  2. C. elegans dystroglycan (DG) DGN-1 functions to maintain the position of lumbar neurons during late embryonic and larval development.

  3. ten-1 (show ODZ1 ELISA Kits) is required for gonadal and pharyngeal basement membrane integrity and acts redundantly with integrin ina-1 and dystroglycan dgn-1

Xenopus laevis Dystroglycan 1 (Dystrophin-Associated Glycoprotein 1) (DAG1) interaction partners

  1. Dystroglycan is involved in skin morphogenesis downstream of the Notch (show NOTCH1 ELISA Kits) signaling pathway

  2. Dystroglycan is required for proper retinal layering

  3. These data indicate that dystroglycan plays a key role for laminin-1 (show LAMA1 ELISA Kits) assembly and pronephric cell anchoring to the basement membrane during early development of the pronephros.

  4. Results show that dystroglycan is critical for both proliferation and elongation of somitic cells and that the Dg-cytoplasmic domain is required for laminin assembly at intersomitic boundaries.

Mouse (Murine) Dystroglycan 1 (Dystrophin-Associated Glycoprotein 1) (DAG1) interaction partners

  1. Fktn (show FKTN ELISA Kits) deficient mice express moderate to severe muscular dystrophy; glycosylated alpha-dystroglycan has a unique role in muscle regeneration in these mice

  2. 5-amino-4-imidazolecarboxamide riboside treatment increases utrophin (show UTRN ELISA Kits) A and beta-dystroglycan expression in mdx (show DMD ELISA Kits) mouse muscle.

  3. Phosphorylation within the cysteine-rich region of dystrophin (show DMD ELISA Kits) enhances its association with beta-dystroglycan and identifies a potential novel therapeutic target for skeletal muscle wasting.

  4. Results suggest that by interfering in the cross-talk between the transmembrane form of the laminin receptor dystroglycan and F-actin, AHNAK1 (show AHNAK ELISA Kits) influences the cytoskeleton organization of Schwann cells

  5. We evaluate the key characteristics of the mdx in comparison with other mouse mutants with inactivations in DAPC components, along with key modifiers of the disease phenotype.

  6. results indicate a novel role for laminin-dystroglycan interactions in the cooperative integration of astrocytes, endothelial cells, and pericytes in regulating the Blood Brain Barrier.

  7. Endogenous glucuronyltransferase activity of LARGE or LARGE2 (show GYLTL1B ELISA Kits) required for functional modification of alpha-dystroglycan in cells and tissues.

  8. Beta-dystroglycan can respond to ezrin (show EZR ELISA Kits) driven cytoskeletal and cell morphology changes,by translocating from the cytoplasm to the nucleus.

  9. Alpha dystroglycan is a perlecan (show HSPG2 ELISA Kits) receptor that specifically functions in the stellate reticulum of the embryonic stage.

  10. The study provides evidence for at least three separate pools of dystroglycan complexes within myofibers that differ in composition and are differentially affected by loss of dystrophin (show DMD ELISA Kits).

Human Dystroglycan 1 (Dystrophin-Associated Glycoprotein 1) (DAG1) interaction partners

  1. Phosphorylation within the cysteine-rich region of dystrophin (show DMD ELISA Kits) enhances its association with beta-dystroglycan and identifies a potential novel therapeutic target for skeletal muscle wasting.

  2. Novel mutations in DAG1 are associated with asymptomatic hyperCKemia with hypoglycosylation of alpha-dystroglycan.

  3. Depletion of DAG resulted in altered morphology and reduced properties of differentiated HL-60 cells, including chemotaxis, respiratory burst, phagocytic activities and markers of differentiation, implicating DAG as a protein involved in differentiation.

  4. A report of a homozygous novel DAG1 missense mutation c.2006G>T in the beta-subunit (show POLG ELISA Kits) of dystroglycan in two Libyan siblings with with a novel muscle-eye-brain disease-like phenotype with multicystic leucodystrophy.

  5. The study provides evidence for at least three separate pools of dystroglycan complexes within myofibers that differ in composition and are differentially affected by loss of dystrophin (show DMD ELISA Kits).

  6. These data suggest that proteolysis, tyrosine phosphorylation and translocation of dystroglycan to the nucleus resulting in altered gene transcription could be important mechanisms in the progression of prostate cancer.

  7. T192M point-mutation in dystroglycan leads to a weaker interactions with laminin-1 (show LAMA1 ELISA Kits), which leads to hypoglycosylation and which finally leads to the limb girdle disease.

  8. GTDC2 generates CTD110.6 antibody-reactive N-acetylglucosamine epitopes on the O-mannosylated alpha-dystroglycan.

  9. the Dystroglycan-mediated cortical microtubule anchoring, the disruption of which initiates gastrulation EMT (show ITK ELISA Kits).

  10. Loss of alpha-dystroglycan and increased CD133 expression are frequent events in human colon cancer and evaluation of CD133 expression could help to identify high-risk colon cancer patients.

Rabbit Dystroglycan 1 (Dystrophin-Associated Glycoprotein 1) (DAG1) interaction partners

  1. Results provide evidence that MMP-2 (show MMP2 ELISA Kits) bears the potentiality to cleave alpha-DG enriched from rabbit skeletal muscle indicating that this degradation indeed might also occur in vivo.

Dystroglycan 1 (Dystrophin-Associated Glycoprotein 1) (DAG1) Antigen Profile

Antigen Summary

Dystroglycan is a laminin binding component of the dystrophin-glycoprotein complex which provides a linkage between the subsarcolemmal cytoskeleton and the extracellular matrix. Dystroglycan 1 is a candidate gene for the site of the mutation in autosomal recessive muscular dystrophies. The dramatic reduction of dystroglycan 1 in Duchenne muscular dystrophy leads to a loss of linkage between the sarcolemma and extracellular matrix, rendering muscle fibers more susceptible to necrosis. Dystroglycan also functions as dual receptor for agrin and laminin-2 in the Schwann cell membrane. The muscle and nonmuscle isoforms of dystroglycan differ by carbohydrate moieties but not protein sequence. Alternative splicing results in multiple transcript variants all encoding the same protein.

Gene names and symbols associated with DAG1

  • dystroglycan 1 (dystrophin-associated glycoprotein 1) (Dag1) antibody
  • dystroglycan 1 (dystrophin-associated glycoprotein 1) (DAG1) antibody
  • dystroglycan-like (LOC100620392) antibody
  • Dystroglycan (Dg) antibody
  • DystroGlycaN (dgn-1) antibody
  • DystroGlycaN (dgn-3) antibody
  • DystroGlycaN (dgn-2) antibody
  • dystroglycan 1 (dag1) antibody
  • dystroglycan (LOC398500) antibody
  • dystroglycan (Dg) antibody
  • dystroglycan 1 (dystrophin-associated glycoprotein 1) (dag1) antibody
  • dystroglycan 1 (Dag1) antibody
  • 156DAG antibody
  • A3a antibody
  • AGRNR antibody
  • atu antibody
  • CG18250 antibody
  • CT41273 antibody
  • D9Wsu13e antibody
  • DAG antibody
  • DAG1 antibody
  • dg antibody
  • dgn antibody
  • DmDG antibody
  • Dmel\\CG18250 antibody
  • Dp71 antibody
  • Dp427 antibody
  • dys antibody
  • GB14967 antibody
  • LOC398500 antibody
  • MDDGC7 antibody
  • MDDGC9 antibody
  • MGC53537 antibody
  • RAB7 antibody

Protein level used designations for DAG1

dystroglycan , CG18250-PA , CG18250-PB , CG18250-PC , CG18250-PD , Dg-PA , Dg-PB , Dg-PC , Dg-PD , atsugari , dystroglycan-like , DystroGlycaN family member (dgn-1) , DystroGlycaN family member (dgn-3) , DystroGlycaN family member (dgn-2) , dystroglycan 1 , dystroglycan 1 (dystrophin-associated glycoprotein 1) , alpha-dystroglycan , beta-dystroglycan , dystrophin associated glycoprotein 1 , RAB7, member RAS oncogene family , dystrophin-associated glycoprotein 1 , glycine cleavage system T-protein

GENE ID SPECIES
114489 Rattus norvegicus
100049058 Gallus gallus
100053150 Equus caballus
100620392 Sus scrofa
36773 Drosophila melanogaster
181283 Caenorhabditis elegans
184149 Caenorhabditis elegans
186365 Caenorhabditis elegans
380447 Xenopus laevis
398500 Xenopus laevis
408826 Apis mellifera
460372 Pan troglodytes
549272 Xenopus (Silurana) tropicalis
100395530 Callithrix jacchus
100579781 Nomascus leucogenys
13138 Mus musculus
1605 Homo sapiens
281439 Bos taurus
476623 Canis lupus familiaris
100009278 Oryctolagus cuniculus
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