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.
ASPM
abnormal spindle microtubule assembly
Abnormal spindle-like microcephaly-associated protein
:  Abnormal spindle protein homolog ASP asp (abnormal spindle) homolog, microcephaly associated asp (abnormal spindle) homolog, microcephaly associated (Drosophila) asp (abnormal spindle)-like, microcephaly associated (Drosophila) Asp homolog Calmbp1 FLJ10517 FLJ10549 MCPH5 microcephaly, primary autosomal recessive 5 More... Less...
Product
Specifications
Ordering Information
Human
ICC, IF
$360
$99