You are viewing an incomplete version of our website. Please click to reload the website as full version.

Serine/threonine Kinase 19, Pseudogene 1 Proteins (STK19-PS1)

The RP2 locus has been implicated as one cause of X-linked retinitis pigmentosa. Additionally we are shipping Serine/threonine Kinase 19, Pseudogene 1 Antibodies (31) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
STK19-PS1 6102 O75695
Rat STK19-PS1 STK19-PS1 140662 P02401
Mouse STK19-PS1 STK19-PS1 114241  
How to order from antibodies-online
  • +1 877 302 8632
  • +1 888 205 9894 (toll-free)
  • Order online
  • orders@antibodies-online.com

Top Serine/threonine Kinase 19, Pseudogene 1 Proteins at antibodies-online.com

Showing 4 out of 5 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
HOST_Escherichia coli (E. coli) Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 29 to 34 Days
$4,331.68
Details
HOST_Wheat germ Human GST tag 10 μg Log in to see 9 Days
$405.71
Details
HOST_Baculovirus infected Insect Cells Human GST tag 100 μg Log in to see 16 Days
$822.80
Details
HOST_Human Human Un-conjugated   20 μg Log in to see 9 to 11 Days
$785.40
Details

STK19-PS1 Proteins by Origin and Source

Origin Expressed in Conjugate
Human , , ,
,

More Proteins for Serine/threonine Kinase 19, Pseudogene 1 (STK19-PS1) Interaction Partners

Human Serine/threonine Kinase 19, Pseudogene 1 (STK19-PS1) interaction partners

  1. The ability of the restored RP2 protein (show P2RX1 Proteins) level to reverse the observed cellular phenotypes in cells lacking RP2 (show NUDT19 Proteins) indicates that translational read-through could be clinically beneficial for patients.

  2. ellipsometric measurements of naRP2 demonstrated that its particular affinity for saturated phospholipids can be explained by its larger extent of insertion in this phospholipid monolayer compared to that in polyunsaturated phospholipid monolayers.

  3. The methylation state of CpG sites close to the RP2 (show NUDT19 Proteins) core promoter (GAAA)n repeat serves as a proxy measurement of X-chromosome inactivation in human and non-human primates.

  4. A novel frameshift mutation in RP2 (show NUDT19 Proteins) was detected. This mutation was located in exon 2 of the RP2 (show NUDT19 Proteins) gene: a nucleotide C was inserted at 111 (c.111insC, Fig. 1A), which caused a protein translation frameshift

  5. Direct sequencing of RPGR (show RPGR Proteins) and RP2 (show NUDT19 Proteins) allowed for identification of a disease-causing mutation in 21 families. Of these "adRP (show PLIN2 Proteins)" families 19 had RPGR (show RPGR Proteins) mutations, and two had RP2 (show NUDT19 Proteins) mutations.

  6. Based on our findings, we suggest that RPGR (show RPGR Proteins) should be considered as a first tier gene for screening isolated males with retinal degeneration.

  7. data support a role for RP2 in facilitating the membrane association and traffic of Gbeta1, potentially prior to the formation of the obligate Gbeta:Ggamma heterodimer; combined with other recent evidence, this suggests that RP2 may co-operate with Arl3 and its effectors in the cilia-associated traffic of G proteins

  8. The localization of RP2 (show NUDT19 Proteins) to basal bodies and cilia in photoreceptors and kidney cells has linked RP2 (show NUDT19 Proteins) dysfunction with ciliopathies.

  9. Data demonstrate that Importin (show KPNA4 Proteins) beta2 is necessary for localization of retinitis pigmentosa 2 (RP2 (show NUDT19 Proteins)) to the primary cilium, and identify two distinct binding sites of RP2 (show NUDT19 Proteins), which interact independently with Importin (show KPNA4 Proteins) beta2.

  10. An identifiable phenotype for RP2 (show NUDT19 Proteins)-X-linked retinitis pigmentosa aids in clinical diagnosis and targeted genetic screening.

Serine/threonine Kinase 19, Pseudogene 1 (STK19-PS1) Protein Profile

Protein Summary

The RP2 locus has been implicated as one cause of X-linked retinitis pigmentosa. The predicted gene product shows homology with human cofactor C, a protein involved in the ultimate step of beta-tubulin folding. Progressive retinal degeneration may therefore be due to the accumulation of incorrectly-folded photoreceptor or neuron-specific tubulin isoforms followed by progressive cell death

Gene names and symbols associated with STK19-PS1

  • retinitis pigmentosa 2 (X-linked recessive) (RP2)
  • ribosomal protein, large P2 (Rplp2)
  • serine/threonine kinase 19, pseudogene 1 (Stk19-ps1)
  • DELXp11.3 protein
  • NM23-H10 protein
  • NME10 protein
  • RP2 protein
  • TBCCD2 protein
  • XRP2 protein

Protein level used designations for STK19-PS1

protein XRP2 , 60S acidic ribosomal protein P2 , ribosomal protein P2

GENE ID SPECIES
6102 Homo sapiens
140662 Rattus norvegicus
114241 Mus musculus
Selected quality suppliers for Serine/threonine Kinase 19, Pseudogene 1 Proteins (STK19-PS1)
Did you look for something else?