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Protocadherin 19 Proteins (PCDH19)

The protein encoded by PCDH19 is a member of the delta-2 protocadherin subclass of the cadherin superfamily. Additionally we are shipping Protocadherin 19 Antibodies (14) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
PCDH19 57526 Q8TAB3
PCDH19 279653 Q80TF3
Rat PCDH19 PCDH19 317183  
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Top Protocadherin 19 Proteins at antibodies-online.com

Showing 3 out of 7 products:

Catalog No. Origin Source Conjugate Images Quantity Supplier Delivery Price Details
Insect Cells Human His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 59 Days
$7,759.50
Details
Insect Cells Mouse His tag „Crystallography Grade“ protein due to multi-step, protein-specific purification process 1 mg Log in to see 59 Days
$7,759.50
Details
HOST_Wheat germ Human GST tag   25 μg Log in to see 9 Days
$552.72
Details

PCDH19 Proteins by Origin and Source

Origin Expressed in Conjugate
Human ,
, ,
Mouse (Murine)
,

More Proteins for Protocadherin 19 (PCDH19) Interaction Partners

Human Protocadherin 19 (PCDH19) interaction partners

  1. mild tonic, fluttering and mild clonic phases were most characteristic of seizures of PCDH19-related epilepsy

  2. The study demonistrated that most effective drugs in patients with PCDH19 mutations were bromide and clobazam.

  3. PCDH19 has a role in instructing the apico-basal polarity of the progenitor cells, thus regulating the development of a properly organized human brain

  4. Two mosaic PCDH19 point mutations are described in male patients with PCDH19-related epilepsy.

  5. steroids and in particular neurosteroids (e.g. allopregnanolone) play an important role in PCDH19-FE and represent a realistic therapeutic target.

  6. This case report is suggestive of a good response of PCDH19-related Epilepsy to stiripentol

  7. This study proposes corticosteroid treatment as an efficacious adjunctive treatment for the acute symptoms of PCDH19-Generalized Convulsive Epilepsy and suggests BBB involvement in this disease.

  8. analysis of four novel mutations in the PCDH19 gene found in isolated cases of girls with infantile onset epilepsy

  9. The present findings confirm that PCDH19 is a major causative gene for infantile onset familial or sporadic epilepsy in female patients with or without mental retardation.

  10. girls with a de novo mutation in PCDH19 presented a delay of expressive language acquisition and lower scores at follow-up testing completed at older ages

Mouse (Murine) Protocadherin 19 (PCDH19) interaction partners

  1. Pcdh19 gene is developmentally regulated during mouse organogenesis and shows a unique expression profile among protocadherins.

Protocadherin 19 (PCDH19) Protein Profile

Protein Summary

The protein encoded by this gene is a member of the delta-2 protocadherin subclass of the cadherin superfamily. The encoded protein is thought to be a calcium-dependent cell-adhesion protein that is primarily expressed in the brain. Defects in this gene are a cause of epilepsy female-restricted with mental retardation (EFMR). Three transcript variants encoding different isoforms have been found for this gene.

Gene names and symbols associated with Protocadherin 19 Proteins (PCDH19)

  • protocadherin 19 (PCDH19)
  • protocadherin 19 (Pcdh19)
  • B530002L05Rik protein
  • EFMR protein
  • EIEE9 protein
  • Gm717 protein
  • mKIAA1313 protein
  • RGD1565392 protein

Protein level used designations for Protocadherin 19 Proteins (PCDH19)

protocadherin-19

GENE ID SPECIES
57526 Homo sapiens
279653 Mus musculus
317183 Rattus norvegicus
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