PKD1 Polyclonal Antibody
€0.00
In stock
SKU
E-AB-15660
Catalog Number: E-AB-15660
Isotype: Rabbit IgG
Reactivity: human, mouse
Applications: IHC,ELISA
Datasheet, Questions? Contact us!
Isotype: Rabbit IgG
Reactivity: human, mouse
Applications: IHC,ELISA
Datasheet, Questions? Contact us!
Background:
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).
Research Area: Cancer, Metabolism, Signal Transduction
Synonyms:
Autosomal dominant polycystic kidney disease 1 protein, Autosomal dominant polycystic kidney disease protein 1, nPKC-D1, nPKC-mu, OTTHUMP00000208669, OTTHUMP00000208670, PBP, Pc-1, PKD, Pkd1, PKD1, Polycystic Kidney Disease 1, polycystic kidney disease-associated protein, Polycystin 1 Precursor, Polycystin-1, Protein kinase C mu type, Protein kinase D, Serine/threonine-protein kinase D1, transient receptor potential cation channel, subfamily P, member 1, TRPP1
Immunogen: Synthetic peptide of human PKD1
Swissprot: P98161
Gene Accession: NP_001009944
Purification Method: Affinity purification
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Concentration: 0.6 mg/mL
Dilution: IHC 1:50-1:200
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
Alternative for product with catalog number:
sc-10371/sc-10372/sc-10370/sc-25570
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).
Research Area: Cancer, Metabolism, Signal Transduction
Synonyms:
Autosomal dominant polycystic kidney disease 1 protein, Autosomal dominant polycystic kidney disease protein 1, nPKC-D1, nPKC-mu, OTTHUMP00000208669, OTTHUMP00000208670, PBP, Pc-1, PKD, Pkd1, PKD1, Polycystic Kidney Disease 1, polycystic kidney disease-associated protein, Polycystin 1 Precursor, Polycystin-1, Protein kinase C mu type, Protein kinase D, Serine/threonine-protein kinase D1, transient receptor potential cation channel, subfamily P, member 1, TRPP1
Immunogen: Synthetic peptide of human PKD1
Swissprot: P98161
Gene Accession: NP_001009944
Purification Method: Affinity purification
Buffer: PBS with 0.05% sodium azide and 50% glycerol, PH7.4
Concentration: 0.6 mg/mL
Dilution: IHC 1:50-1:200
Storage:
Store at -20°C. Avoid freeze / thaw cycles.
Alternative for product with catalog number:
sc-10371/sc-10372/sc-10370/sc-25570
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