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anti-Eyes Shut Homolog (Drosophila) (EYS) Antibodies

The product of EYS contains multiple epidermal growth factor (EGF)-like and LamG domains. Additionally we are shipping and many more products for this protein.

list all antibodies Gene Name GeneID UniProt
EYS 346007 Q5T1H1
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Top anti-EYS Antibodies at

Showing 3 out of 4 products:

Catalog No. Reactivity Host Conjugate Application Images Quantity Supplier Delivery Price Details
Human Mouse Un-conjugated ELISA, WB Detection limit for recombinant GST tagged EYS is 0.3 ng/ml as a captu... Western Blot detection against Immunogen (36.63 KDa) . 100 μg Log in to see 9 Days
Human Mouse Un-conjugated ELISA, WB EYS polyclonal antibody (A01), Lot # 051205JC01 Western Blot analysis ... Western Blot detection against Immunogen (37 KDa) . 50 μL Log in to see 9 Days
Human Mouse Un-conjugated ELISA, WB   100 μg Log in to see 11 to 16 Days

EYS Antibodies by Reactivity, Application, Clonality and Conjugate

Attributes Applications Host Clonality


More Antibodies against EYS Interaction Partners

Human Eyes Shut Homolog (Drosophila) (EYS) interaction partners

  1. our study expands the genotypic spectrums for EYS mutations, and may provide novel insights into the relevant pathogenesis for RP. We also demonstrate targeted next-generation sequencing approach as a valuable tool for genetic diagnosis.

  2. New variants were found to be located on the USH2A (show USH2A Antibodies), RPGR (show RPGR Antibodies), EYS, and RHO genes

  3. Advanced retinal degenerative changes with near-total absence of rods and preservation of some perifoveal cones are observed in arRP donor retinas with EYS mutations.

  4. We confirmed with our previous findings that PTP4A1 (show PTP4A1 Antibodies)-PHF3-EYS variants were significantly associated with alcohol dependence.

  5. Our results demonstrated that EYS mutations can be the cause of not only autosomal recessive retinitis pigmentosa but also autoisomal recessive cone-rod dystrophy.

  6. PTP4A1 (show PTP4A1 Antibodies)-PHF3-EYS variants were associated with alcohol dependence.

  7. This study was conducted to determine the spectrum and frequency of EYS mutations in 100 Japanese autosomal recessive retinitis pigmentosa patients.

  8. One-third of Japanese patients with nonsyndromic autosomal recessive retinitis pigmentosa carried probable pathogenic mutations in the EYS gene, including two founder mutations

  9. The results of this GWAS, replication, and fine mapping study provide the first reported evidence that genetic variants mutation within the EYS gene, may be associated with severe statin myopathy.

  10. Results suggest that midsized genomic rearrangements in EYS gene would be a common event in the appearance of retinitis pigmentosa phenotype

EYS Antigen Profile

Protein Summary

The product of this gene contains multiple epidermal growth factor (EGF)-like and LamG domains. The protein is expressed in the photoreceptor layer of the retina, and the gene is mutated in autosomal recessive retinitis pigmentosa. Multiple transcript variants encoding different isoforms have been found for this gene.

Gene names and symbols associated with EYS

  • eyes shut homolog (Drosophila) (EYS) antibody
  • bA74E24.1 antibody
  • bA166P24.2 antibody
  • bA307F22.3 antibody
  • C6orf178 antibody
  • C6orf179 antibody
  • C6orf180 antibody
  • dJ22I17.2 antibody
  • dJ303F19.1 antibody
  • dJ1018A4.2 antibody
  • EGFL10 antibody
  • EGFL11 antibody
  • RP25 antibody
  • SPAM antibody

Protein level used designations for EYS

EGF-like-domain, multiple 10 , EGF-like-domain, multiple 11 , epidermal growth factor-like protein 10 , epidermal growth factor-like protein 11 , protein eyes shut homolog , protein spacemaker homolog

346007 Homo sapiens
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