Home  >  Products  >  ASPM (ASP (Abnormal Spindle)-like Microcephaly Associated, Microcephaly, Primary Autosomal Recessive 5, HGNC:19048, FLJ10517, FLJ10549, MCPH5)
ASPM (ASP (Abnormal Spindle)-like Microcephaly Associated, Microcephaly, Primary Autosomal Recessive 5, HGNC:19048, FLJ10517, FLJ10549, MCPH5)

ASPM (ASP (Abnormal Spindle)-like Microcephaly Associated, Microcephaly, Primary Autosomal Recessive 5, HGNC:19048, FLJ10517, FLJ10549, MCPH5)

Cat no: A3883-40

Supplier: United States Biological
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The ASPM gene is the human ortholog of the Drosophila melanogaster 'abnormal spindle' gene (asp), which is essential for normal mitotic spindle function in embryonic neuroblasts (Bond et al., 2002). The mouse gene Aspm is expressed specifically in the primary sites of prenatal cerebral cortical neurogenesis.[supplied by OMIM] Applications: Suitable for use in Immunohistochemistry and Immunocytochemistry. Other applications not tested. Recommended Dilution: Optimal dilutions to be determined by the researcher. Storage and Stability: May be stored at 4 degrees C for short-term only. For long-term storage and to avoid repeated freezing and thawing, aliquot Store at -20 degrees C. Aliquots are stable for at least 12 months at -20 degrees C. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap. Further dilutions can be made in assay buffer.
Catalogue number: A3883-40
Reactivities: Human
Hosts: Rabbit
Applications: Immunocytochemistry, Immunohistochemistry
Size: 100ul
Form: Supplied as a liquid in TBS, pH 7.2, 0.1% BSA, 0.1% sodium azide.
P type: Pab
Purity: Purified by immunoaffinity chromatography.
Alternative names: Asp (abnormal spindle) Homolog, Microcephaly Associated
Additional info: Species Crossreactivity: Human. Other species have not been tested.

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