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Rabbit Anti-MYH9/FITC Conjugated antibody
background:
Cellular myosin that appears to play a role in cytokinesis, cell shape, and specialized functions such as secretion and capping.
Defects in MYH9 are the cause of May-Hegglin anomaly (MHA) . MHA is an autosomal dominant macrothrombocytopenia characterized by thrombocytopenia, giant platelets and leukokyte inclusions appearing as highly parallel paracrystalline bodies.
Function:
Cellular myosin that appears to play a role in cytokinesis, cell shape, and specialized functions such as secretion and capping.
Subunit:
Interacts with PDLIM2. Interacts with SLC6A4. Myosin is a hexameric protein that consists of 2 heavy chain subunits (MHC), 2 alkali light chain subunits (MLC) and 2 regulatory light chain subunits (MLSLC2). Interacts with RASIP1. Interacts with DDR1. Interacts with SVIL and HTRA3.
Subcellular Location:
Cytoplasm, cytoskeleton. Cytoplasm, cell cortex.
Tissue Specificity:
In the kidney, expressed in the glomeruli. Also expressed in leukocytes.
Post-translational modifications:
ISGylated.
Similarity:
Contains 1 IQ domain.
Contains 1 myosin head-like domain.
Database links:
Entrez Gene: 4627 Human
Entrez Gene: 17886 Mouse
Entrez Gene: 25745 Rat
Omim: 160775 Human
SwissProt: P35579 Human
SwissProt: Q8VDD5 Mouse
SwissProt: Q62812 Rat
Unigene: 474751 Human
Unigene: 29677 Mouse
Unigene: 2285 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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