« Back
Home /
Phospho-MYH9(Y158) Blocking Peptide

Phospho-MYH9(Y158) Blocking Peptide

Manufacturer	Abcepta
Category	Peptides & Proteins Peptides
Type	Peptides
Specific against	other
Format	Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
Amount	500 ug
Item no.	ABC-BP3775a
eClass 6.1	34160400
eClass 9.0	32160409
Available
Primary Accession	P35579
Bio Background	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.
Bio References	Arii, J., et al. Nature 467(7317):859-862(2010) Genovese, G., et al. Kidney Int. 78(7):698-704(2010) Tzur, S., et al. Hum. Genet. 128(3):345-350(2010) Bostrom, M.A., et al. Hum. Genet. 128(2):195-204(2010) Oleksyk, T.K., et al. PLoS ONE 5 (7), E11474 (2010) :
Gene ID	4627
Gene Name	MYH9
Subtitle	Synthetic peptide
Other Accession	Q62812; Q8VDD5; P14105; NP_002464.1
Target/Specificity	The synthetic peptide sequence is selected from aa 149-165 of HUMAN MYH9

Note: The presented information and documents (Manual, Product Datasheet, Safety Datasheet and Certificate of Analysis) correspond to our latest update and should serve for orientational purpose only. We do not guarantee the topicality. We would kindly ask you to make a request for specific requirements, if necessary.

All products are intended for research use only (RUO). Not for human, veterinary or therapeutic use.

Request Data Sheet

ABC-BP3775a-datasheet.pdf

Request safety datasheet

Simple Order Order Subscription

Amount: 500 ug

available

Delivery expected until 7/4/2024