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Rabbit Anti-GPSM2/FITC Conjugated antibody
background:
Plays an important role in spindle pole orientation. Interacts and contributes to the functional activity of G(i) alpha proteins. Acts to stabilize the apical complex during neuroblast divisions.
Function:
lays an important role in spindle pole orientation. Interacts and contributes to the functional activity of G(i) alpha proteins. Acts to stabilize the apical complex during neuroblast divisions.
Subunit:
Interacts with LLGL2. Interacts with INSC/inscuteable and probably with F2RL2.
Subcellular Location:
Cytoplasm. Cytoplasm, cell cortex. Note=Localizes in the cytoplasm in the interphase and at cell periphery in the metaphase.
Tissue Specificity:
Ubiquitously expressed.
Post-translational modifications:
Defects in GPSM2 are the cause of Chudley-McCullough syndrome (CMCS) [MIM:604213]. An autosomal recessive neurologic disorder characterized by early-onset sensorineural deafness and specific brain anomalies on MRI, including hypoplasia of the corpus callosum, enlarged cysterna magna with mild focal cerebellar dysplasia, and nodular heterotopia. Some patients have hydrocephalus. Psychomotor development is normal.
Similarity:
Belongs to the GPSM family.
Contains 4 GoLoco domains.
Contains 8 TPR repeats.
Database links:
Entrez Gene: 29899 Human
Entrez Gene: 76123 Mouse
Entrez Gene: 362021 Rat
Omim: 609245 Human
SwissProt: P81274 Human
SwissProt: Q8VDU0 Mouse
Unigene: 584901 Human
Unigene: 658489 Human
Unigene: 226941 Mouse
Unigene: 144235 Rat
Important Note:
This product as supplied is intended for research use only, not for use in human, therapeutic or diagnostic applications.
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