Rabbit anti-ASPM IHC Antibody Affinity Purified
Catalog #
ASPM
Human
ICC-IF
Rabbit
Polyclonal
Whole IgG
Between 3425 and C-term
IgG
Unconjugated
Antigen Affinity Purified
Product Details
Human
Human
2 - 8 °C
1 year from date of receipt
Antibody was affinity purified using an epitope specific to ASPM immobilized on solid support.
The epitope recognized by IHC-00058 maps to a region between residue 3425 and the C-terminus (residue 3477) of human ASP (Abnormal Spindle)-like, Microcephaly Associated using the numbering given in entry NP_060606.2 (GeneID 259266).
Antibody was affinity purified using an epitope specific to ASPM immobilized on solid support.
The epitope recognized by IHC-00058-T maps to a region between residue 3425 and the C-terminus (residue 3477) of human ASP (Abnormal Spindle)-like, Microcephaly Associated using the numbering given in entry NP_060606.2 (GeneID 259266).
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.
Abnormal spindle-like microcephaly-associated protein
Alternate Names
Abnormal spindle protein homolog; abnormal spindle-like microcephaly-associated protein; ASP; asp (abnormal spindle) homolog, microcephaly associated; Asp homolog; Calmbp1; MCPH5
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