anti-Sarcoglycan, epsilon (SGCE) Antibodies

SGCE encodes the epsilon member of the sarcoglycan family. Additionally we are shipping SGCE Proteins (7) and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
SGCE 8910 O43556
SGCE 20392 O70258
SGCE 432360 Q6YAT4
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Top anti-SGCE Antibodies at antibodies-online.com

Showing 10 out of 29 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Cow Rabbit Un-conjugated IHC, WB Sample Type: Mouse CerebellumDilution: 1:500 100 μL Log in to see 2 to 3 Days
$289.00
Details
Chicken Rabbit Un-conjugated IHC (p), WB Human Skeletal Muscle: Formalin-Fixed, Paraffin-Embedded (FFPE) 50 μg Log in to see 7 to 9 Days
$676.50
Details
Human Rabbit Un-conjugated ELISA, WB 50 μg Log in to see 2 to 3 Days
$433.13
Details
Human Rabbit Un-conjugated IHC, IHC (p), WB Western Blot: SGCE Antibody [NBP2-20335] - Sample (30 ug of whole cell lysate) A: Hela 10% SDS PAGE gel, diluted at 1:1000. Immunohistochemistry-Paraffin: SGCE Antibody [NBP2-20335] - Immunohistochemical analysis of paraffin-embedded ES2 xenograft, using antibody at 1:100 dilution. 0.1 mL Log in to see 8 to 11 Days
$447.56
Details
Human Rabbit Un-conjugated IF, IHC, WB 100 μL Log in to see 16 Days
$323.13
Details
Human Rabbit Un-conjugated WB SGCE Antibody (C-term) (ABIN1881798) western blot analysis in A2058 cell line lysates (35 µg/lane). This demonstrates the SGCE antibody detected the SGCE protein (arrow). 400 μL Log in to see 10 to 11 Days
$324.50
Details
Human Rabbit Un-conjugated ICC, IF, WB Western Blot: SGCE Antibody  - Western blot analysis in human cell line RT-4, human cell line U-251 MG, human plasma, human liver tissue and human tonsil tissue. Immunocytochemistry/Immunofluorescence: SGCE Antibody  - Staining of human cell line SK-MEL-30 shows localization to nucleoplasm, plasma membrane & vesicles. 100 μL Log in to see 10 to 13 Days
$439.69
Details
Human Rabbit Un-conjugated IC, IF, IHC, WB Immunofluorescent analysis of Epsilon-sarcoglycan staining in Hela cells. Formalin-fixed cells were permeabilized with 0.1% Triton X-100 in TBS for 5-10 minutes and blocked with 3% BSA-PBS for 30 minutes at room temperature. Cells were probed with the pri Immunohistochemical analysis of Epsilon-sarcoglycan staining in mouse heart formalin fixed paraffin embedded tissue section. The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0). The section was then incuba 200 μL Log in to see 13 to 14 Days
$487.50
Details
Human Rabbit Un-conjugated IHC, ELISA, WB   100 μg Log in to see 7 to 9 Days
$478.50
Details
Human Rabbit Un-conjugated IHC, IHC (p), WB Immunohistochemistry-Paraffin: SGCE Antibody [NBP1-59794] - Mouse cerebellum tissue, 1:500 dilution. Western Blot: SGCE Antibody [NBP1-59794] - Sample Type: 721_B Antibody Dilution: 1.0 ug/ml SGCE is supported by BioGPS gene expression data to be expressed in 721_B 100 μL Log in to see 8 to 11 Days
$447.56
Details

SGCE Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality
Human
,

Mouse (Murine)


Rat (Rattus)


More Antibodies against SGCE Interaction Partners

Human Sarcoglycan, epsilon (SGCE) interaction partners

  1. SGCE mutation can cause a broad range of clinical symptoms between and within families. We should consider MDS (show PAFAH1B1 Antibodies) as a differential diagnosis for patients with paroxysmal walking abnormalities and/or myoclonic movements.

  2. Tata confirms that SGCE mutations are most commonly identified in Myoclonus dystonia syndrome patients with (1) age at onset

  3. found one patient with a novel heterozygous frameshift mutation in the DYT11 gene

  4. The co-occurrence of seizures and myoclonus-dystonia suggests that they are both due to the same underlying SGCE mutation

  5. A novel frameshift mutation of the SGCE gene in an Iranian family with Myoclonus-dystonia syndrome confirming the variability of the clinical symptoms caused by the same mutation within members of a family.

  6. In myoclonus-dystonia syndrome patients a substantial mutation in exon 3 of SGCE gene was found.

  7. The results of this study suggested performing gene dosage analysis by multiple ligation-dependent probe amplification (MLPA) to individuate large SGCE deletions that can be responsible for complex phenotypes.

  8. SGCE mutations are associated with a specific psychiatric phenotype consisting of compulsivity, anxiety and alcoholism in addition to the characteristic motor phenotype.

  9. Although reduced penetrance in DYT11-MD has been attributed to the maternal imprinting epsilon-sarcoglycan mutations, NM-DYT11 carriers showed significant metabolic abnormalities that are not explained by this genetic model.

  10. anxiety disorders and executive dysfunctions may be part of the phenotype of myoclonus-dystonia patients with a DYT11 mutation

Pig (Porcine) Sarcoglycan, epsilon (SGCE) interaction partners

Mouse (Murine) Sarcoglycan, epsilon (SGCE) interaction partners

  1. The results suggest that varepsilon-sarcoglycan (show SGCD Antibodies) in the cerebellar Purkinje cells contributes to the motor learning, while loss of varepsilon-sarcoglycan (show SGCD Antibodies) in other brain regions may contribute to nuclear envelope abnormality, myoclonus and motor coordination deficits.

  2. results suggest that the loss of epsilon-sarcoglycan in the striatum contributes to motor deficits, while it alone does not produce abnormal nuclear envelopes or myoclonus

  3. impaired ectodomain shedding of M68T, a process that occurs physiologically for epsilon-sarcoglycan resulting in the lysosomal trafficking of the intracellular C-terminal domain of the protein. ( epsilon-sarcoglycan )

  4. Sgca-;Sgce-null mouse shows a complete loss of residual sarcoglycans and a strong reduction in both dystrophin and dystroglycan.

  5. Data describe mice carrying mutations in both Dyt1 (show TOR1A Antibodies) and Sgce and show that these double mutant mice show earlier onset of motor deficits in beam-walking test.

  6. Sgce gene is imprinted, with exclusive expression from the paternal allele.

  7. These results suggest that the two epsilon-SG isoforms might play different roles in synaptic functions of the central nervous system.

  8. High expression levels of epsilon-sarcoglycan mRNA and protein were found in the mitral cell layer of the olfactory bulb, the Purkinje cell layer in cerebellum, and the monoaminergic neurons in the mouse midbrain.

  9. diverse symptoms associated with myoclonus-dystonia are indeed resulted from a single SGCE gene mutation that leads to alterations of dopaminergic and serotonergic systems.

  10. Data demonstrate a novel function of the sarcoglycan (show SGCD Antibodies) complex in whole body glucose homeostasis and skeletal muscle metabolism, suggesting that the impairment of the skeletal muscle metabolism influences the pathogenesis of muscular dystrophy.

SGCE Antigen Profile

Protein Summary

This gene encodes the epsilon member of the sarcoglycan family. Sarcoglycans are transmembrane proteins that are components of the dystrophin-glycoprotein complex, which link the actin cytoskeleton to the extracellular matrix. Unlike other family members which are predominantly expressed in striated muscle, the epsilon sarcoglycan is more broadly expressed. Mutations in this gene are associated with myoclonus-dystonia syndrome. This gene is imprinted, with preferential expression from the paternal allele. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

Gene names and symbols associated with SGCE

  • sarcoglycan, epsilon (sgce) antibody
  • sarcoglycan, epsilon (SGCE) antibody
  • sarcoglycan, epsilon (Sgce) antibody
  • DYT11 antibody
  • e-SG antibody
  • ESG antibody
  • scge antibody
  • zgc:92318 antibody

Protein level used designations for SGCE

Epsilon-sarcoglycan , epsilon-sarcoglycan , dystonia 11, myoclonic , epsilon-SG

GENE ID SPECIES
100380447 Salmo salar
368230 Danio rerio
734393 Xenopus laevis
8910 Homo sapiens
475233 Canis lupus familiaris
100240725 Sus scrofa
407209 Bos taurus
20392 Mus musculus
432360 Rattus norvegicus
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