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By Research Area / Cell Cycle / ASPM
 

ASPM Antibody

 
ASPM (abnormal spindle-like microcephaly associated) is also known as MCPH5 (autosomal recessive primary microcephaly 5). Defects in ASPM are the cause of microcephaly primary type 5 or microcephaly vera, an autosomal recessive disease characterized by reduced head circumference, small cerebral cortex, and reduced brain weight. At the cellular level, MCPH5 is important to mitotic spindle function and may play a preferential role in prenatal neurogenesis. Alternate names for ASPM include abnormal spindle protein homolog, Asp homolog, Calmbp1, FLJ10517, FLJ10549, FLJ3117, and DKFZp686N06184.
 
Product / Catalog #SpecificationsPrice
ASPM IHC Antibody
IHC-00058		Applications: ICC
Reactivity: Human
Quantity: 0.1 ml (50 - 250 slides)
$360.00
Data Sheet
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