MYH9 (pY158) 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	MYH9 (pY158)
Clonality	Polyclonal
Target Modification	Tyr158
Modification	Phosphorylation
Reactivity	Human
Tested Applications	ELISA, DB
Host	Rabbit
Recommended dilutions	DB: 1/500. Optimal dilutions/concentrations should be determined by the end user.
Conjugation	Unconjugated
Immunogen	KLH-conjugated synthetic phosphopeptide corresponding to amino acid residues surrounding Y158 of human MYH9.
Isotype	IgG
Form	Liquid
Purification	Purified through a protein A column, followed by two-step phosphospecific 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
KEGG	hsa:4627
String	9606.ENSP00000216181
Molecular Weight	Calculated MW: 227 kDa
Buffer	PBS containing 0.09% sodium azide.
Specificity	Predicted to react with Mouse, Rat and Chicken MYH9.
Availability	Shipped within 5-10 working days.
Note	This product is for research use only.

Research Articles on MYH9 (pY158)

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