Myosin-9 (MYH9) Antibody

This gene encodes a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain. The protein is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in MYH9 are the cause of non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness.

Target	Myosin-9 (MYH9)
Clonality	Polyclonal
Reactivity	Human, Mouse
Tested Applications	ELISA, WB
Host	Rabbit
Recommended dilutions	WB: 1/2000. Optimal dilutions/concentrations should be determined by the end user.
Conjugation	Unconjugated
Immunogen	KLH-conjugated synthetic peptide between 1840-1867 amino acids from the C-terminal region of human MYH9.
Isotype	IgG
Form	Liquid
Purification	Purified through a protein A column, followed by peptide affinity purification.
Storage	Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
UniProt Primary AC	P35579 (UniProt, ExPASy)
UniProt Secondary AC	A8K6E4, O60805, Q60FE2, Q86T83
UniProt Entry Name	MYH9_HUMAN
Gene Symbol	MYH9
GeneID	4627
OMIM	155100
NCBI Accession	NP_002464.1 NM_002473.5
HGNC	7579
KEGG	hsa:4627
Ensembl	ENSG00000100345
String	9606.ENSP00000216181
Molecular Weight	Calculated MW: 227 kDa
Buffer	PBS containing 0.09% sodium azide.
Availability	Shipped within 5-10 working days.
Note	This product is for research use only.

Research Articles on Myosin-9 (MYH9)

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