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Polycystic Kidney Disease 1 (Autosomal Dominant) Proteins (PKD1)

PKD1 encodes a member of the polycystin protein family. Additionally we are shipping Polycystic Kidney Disease 1 (Autosomal Dominant) Antibodies (39) and Polycystic Kidney Disease 1 (Autosomal Dominant) Kits (4) and many more products for this protein.

list all proteins Gene Name GeneID UniProt
PKD1 5310 P98161
Mouse PKD1 PKD1 18763 O08852
Rat PKD1 PKD1 24650  
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Top Polycystic Kidney Disease 1 (Autosomal Dominant) Proteins at

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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 pu... 1 mg Log in to see 29 to 34 Days

PKD1 Proteins by Origin and Source

Origin Expressed in Conjugate

More Proteins for Polycystic Kidney Disease 1 (Autosomal Dominant) (PKD1) Interaction Partners

Human Polycystic Kidney Disease 1 (Autosomal Dominant) (PKD1) interaction partners

  1. Germline mutations in PKD1 gene is associated with autosomal-dominant polycystic kidney disease.

  2. Host cortactin, PKD1 and actin are recruited by Trypanosoma cruzi extracellular amastigotes based on experiments in fixed and live cells by time lapse confocal microscopy.

  3. PCs expression and p53 (show TP53 Proteins) activation as a regulator of cell proliferation were further evaluated in vivo and in 69 advanced human carotid atherosclerotic plaques.

  4. These results suggest that, at least in some patients, the severity of the cystic disease is inversely correlated with the level of polycystin 1 function.

  5. Overexpression of PKD1 in a prostate cancer cell line model resulted in decreased cell proliferation and epithelial mesenchymal transition.

  6. and MMP9 (show MMP9 Proteins) expression in PKD1 constitutively-active MD-MB-231 cells and MCF-7 knockdown cells were decreased and increased respectively

  7. A substantial number of PKD1 missense or synonymous mutations characterize pre-mRNA splicing. One missense and 2 synonymous mutations induce significant defects in pre-mRNA splicing.

  8. PKD1 gene variation plays a disease modifying role in patients diagnosed with ADPKD.

  9. A short segment of chromosome 16 encodes the tumor suppressor gene tuberin as well as the protein polycystin 1 which are responsible for tuberous sclerosis complex type 2 and autosomal-dominant polycystic kidney disease type 1, respectively.

  10. Case Report: polycystic kidney disease with steatocystoma multiplex. PKD1 mutations disrupt keratin 17 (show KRT17 Proteins) polymerization.

Mouse (Murine) Polycystic Kidney Disease 1 (Autosomal Dominant) (PKD1) interaction partners

  1. Our studies demonstrate that PKD1/2 is a key regulator of MVB maturation and exosome secretion, and constitutes a mediator of the DGK alpha (show DGKA Proteins) effect on MVB secretory traffic.

  2. detected a marked increase in the localization of beta-catenin (show CTNNB1 Proteins) in the nucleus of crypt epithelial cells in the ileum of PKD1

  3. PKD1 phosphorylates AMPKalpha2 (show PRKAA2 Proteins) at Ser485/491, thus diminishing AMPK (show PRKAA1 Proteins) activity.

  4. These data potentially explain the severe renal manifestations of the tuberous sclerosis/polycystic kidney disease contiguous gene syndrome and open new perspectives for the use of mTOR (show FRAP1 Proteins) inhibitors in PKD (show PRKD1 Proteins).

  5. Our results show that AKAP13-PKD1 signaling is critical for transcriptional regulation of key contractile, cell death, and metabolic pathways during the development of compensatory hypertrophy in vivo.

  6. PKD1 acts downstream of TGFalpha and Kras, to mediate formation of ductal structures through activation of the Notch (show NOTCH1 Proteins) pathway.

  7. Results reveal that whereas protein kinase D1 (show PRKD1 Proteins) and protein kinase D2 (show PKD2 Proteins) are essential for neuronal polarity, there exists a functional redundancy between the two proteins.

  8. PKD controls synaptic plasticity and learning by regulating actin stability in dendritic spines.

  9. novel protein complex composed of Rabep1, GGA1 (show GGA1 Proteins) and Arl3 is responsible for the sorting and targeting of the polycystin 1 andpolycystin 2 to the cilium.

  10. Polycystin-1 regulation of the microtubule cytoskeleton impacts on the turnover rates of focal adhesions in migrating cells and we link all these properties to the capability of PC-1 to regulate the activation state of Focal Adhesion Kinase.

Polycystic Kidney Disease 1 (Autosomal Dominant) (PKD1) Protein Profile

Protein Summary

This gene encodes a member of the polycystin protein family. The encoded glycoprotein contains a large N-terminal extracellular region, multiple transmembrane domains and a cytoplasmic C-tail. It is an integral membrane protein that functions as a regulator of calcium permeable cation channels and intracellular calcium homoeostasis. It is also involved in cell-cell/matrix interactions and may modulate G-protein-coupled signal-transduction pathways. It plays a role in renal tubular development, and mutations in this gene cause autosomal dominant polycystic kidney disease type 1 (ADPKD1). ADPKD1 is characterized by the growth of fluid-filled cysts that replace normal renal tissue and result in end-stage renal failure. Splice variants encoding different isoforms have been noted for this gene. Also, six pseudogenes, closely linked in a known duplicated region on chromosome 16p, have been described.

Gene names and symbols associated with PKD1

  • polycystic kidney disease 1 (autosomal dominant) (PKD1)
  • polycystic kidney disease 1 homolog (Pkd1)
  • polycystic kidney disease 1 homolog (human) (Pkd1)
  • protein kinase D1 (Prkd1)
  • mFLJ00285 protein
  • PBP protein
  • Pc-1 protein
  • PC1 protein
  • Pkcm protein
  • PKD protein
  • PKD1 protein
  • Prkcm protein
  • TRPP1 protein

Protein level used designations for PKD1

polycystic kidney disease 1 (autosomal dominant) , polycystin 1 , autosomal dominant polycystic kidney disease 1 protein , polycystic kidney disease-associated protein , polycystin-1 , transient receptor potential cation channel, subfamily P, member 1 , polycystic kidney disease protein 1 , autosomal dominant polycystic kidney disease 1 protein homolog , polycystic kidney disease 1 homolog; polycystin-1 , nPKC-D1 , nPKC-mu , protein kinase C mu type , protein kinase C, mu , protein kinase D , serine/threonine-protein kinase D1

416553 Gallus gallus
749291 Pan troglodytes
5310 Homo sapiens
606755 Canis lupus familiaris
100516429 Sus scrofa
18763 Mus musculus
24650 Rattus norvegicus
18760 Mus musculus
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