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PKD1 antibody
PKD1
Reactivity: Human, Mouse
ELISA, IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-PKD1 Antibody
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Target
See all PKD1 Antibodies
PKD1
(Polycystic Kidney Disease 1 (Autosomal Dominant) (PKD1))
Reactivity
All reactivities for PKD1 antibodies
Human, Mouse
Host
All hosts for PKD1 antibodies
Rabbit
Clonality
All clonalities for PKD1 antibodies
Polyclonal
Conjugate
All conjugates for PKD1 antibodies
This PKD1 antibody is un-conjugated
Application
All applications for PKD1 antibodies
ELISA, Immunohistochemistry (IHC)
Characteristics
Polyclonal Antibody
Purification
Affinity purification
Immunogen
Synthetic peptide of human PKD1
Isotype
IgG
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Alternatives
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Application Details
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Application Notes
IHC 1:50-1:200
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
0.2 mg/mL
Buffer
PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for PKD1
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Target
PKD1
(Polycystic Kidney Disease 1 (Autosomal Dominant) (PKD1))
Alternative Name
PKD1 (PKD1 Products )
Synonyms
PBP antibody, Pc-1 antibody, TRPP1 antibody, PC1 antibody, mFLJ00285 antibody, polycystin 1, transient receptor potential channel interacting antibody, polycystin 1, transient receptor poteintial channel interacting antibody, polycystin-1 antibody, PKD1 antibody, Pkd1 antibody, LOC749291 antibody
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).
NCBI Accession
NP_001009944
UniProt
P98161
Pathways
Myometrial Relaxation and Contraction , Maintenance of Protein Location
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