PKD1 Polyclonal Antibody (E-AB-15660)
For research use only.
Verified Samples |
Verified Samples in IHC: Human thyroid cancer, Human breast cancer, Human kidney |
Dilution | IHC 1:50-1:200 |
Isotype | IgG |
Host | Rabbit |
Reactivity | Human, Mouse |
Applications | IHC |
Clonality | Polyclonal |
Immunogen | Synthetic peptide of human PKD1 |
Abbre | PKD1 |
Synonyms | Autosomal dominant polycystic kidney disease 1 protein, Autosomal dominant polycystic kidney disease protein 1, OTTHUMP00000208669, OTTHUMP00000208670, PBP, PKD, PKD1, Pc-1, Pkd1, Polycystic Kidney Disease 1, nPKC-D1, nPKC-mu, polycystic kidney disease-associated pro |
Swissprot | |
Cellular Localization | Membrane. |
Concentration | 0.6 mg/mL |
Buffer | Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol. |
Purification Method | Affinity purification |
Research Areas | Cancer, Metabolism, Signal Transduction |
Conjugation | Unconjugated |
Storage | Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles. |
Shipping | The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended. |
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). |
Other Clones
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Other Formats
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Unconjugated
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