Phospho-MYH9(Y158) Blocking Peptide

Phospho-MYH9(Y158) Blocking Peptide

€363.00
In stock
SKU
AC-BP3775a
Catalog Number: AC-BP3775a
Size: 500 µg
Datasheet
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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.

Other Names:
Myosin-9, Cellular myosin heavy chain, type A, Myosin heavy chain 9, Myosin heavy chain, non-muscle IIa, Non-muscle myosin heavy chain A, NMMHC-A, Non-muscle myosin heavy chain IIa, NMMHC II-a, NMMHC-IIA, MYH9

Target/Specificity:
The synthetic peptide sequence is selected from aa 149-165 of HUMAN MYH9

Gene Name: MYH9

Gene ID: 4627
Primary Accession: P35579
Other Accession: Q62812; Q8VDD5; P14105; NP_002464.1
Format: Peptides are lyophilized in a solid powder format. Peptides can be reconstituted in solution using the appropriate buffer as needed.
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