PCNT Rabbit Polyclonal Antibody
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PCNT Rabbit Polyclonal Antibody
Background:
The protein encoded by this gene binds to calmodulin and is expressed in the centrosome. It is an integral component of the pericentriolar material (PCM) . The protein contains a series of coiled-coil domains and a highly conserved PCM targeting motif called the PACT domain near its C-terminus. The protein interacts with the microtubule nucleation component gamma-tubulin and is likely important to normal functioning of the centrosomes, cytoskeleton, and cell-cycle progression. Mutations in this gene cause Seckel syndrome-4 and microcephalic osteodysplastic primordial dwarfism type II. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2015], disease:Defects in PCNT are the cause of microcephalic osteodysplastic primordial dwarfism type 2 (MOPD2) [MIM:210720]; also known as osteodysplastic primordial dwarfism type 2. Adults with this rare inherited condition have an average height of 100 centimeters and a brain size comparable to that of a 3-month-old baby, but are of near-normal intelligence., function:An integral component of the pericentriolar material (PCM) ., subcellular location:Centrosomal at all stages of the cell cycle. Remains associated with centrosomes following microtubule depolymerization., subunit:Interacts with PCM1. Binds calmodulin., tissue specificity:Expressed in all tissues tested, including placenta, liver, kidney and thymus.Gene Name:
PCNT KIAA0402 PCNT2Gene ID:
5116Swiss Prot:
O95613Host:
RabbitReactivity:
Human, MouseClonality:
PolyclonalConjugation:
UnconjugatedApplications:
IHC, ICC/IFPurification:
Affinity purificationDilution:
IHC 1:50-1:300, ICC/IF 1:50-1:200Form:
LiquidBuffer:
Liquid in PBS containing 50% glycerol, and 0.02% New type preservative N.Modification:
UnmodifiedMolecular Weight:
366kDaStorage Conditions:
Store at 4°C short term. Aliquot and store at -20°C for 12 months. Avoid freeze/thaw cycles.Isotype:
IgG
