MYH9 Antibody
Product Specifications
Background
MYH9 is 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.
NCBI Gene ID
4627
Swiss Prot
P35579
Accession Number
NP_002464
Host
Rabbit
Reactivity
Human
Immunogen
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human MYH9.
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Other
Purification
Antibody is purified by peptide affinity chromatography method.
Positive Control
Cat. No. 1219 - MCF7 Cell Lysate
Concentration
Batch dependent
Buffer
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
For short periods of storage (days) store at 4˚ C. For longer periods of storage, store MYH9 antibody at -20˚ C. As with any antibody avoid repeat freeze-thaw cycles.
Product Datasheet
https://www.prosci-inc.com/?datasheet_sku=26-280
Calculated Molecular Weight
226 kDa
Applications Notes
MYH9 antibody can be used for detection of MYH9 by ELISA at 1:2500. MYH9 antibody can be used for detection of MYH9 by western blot at 1 μ g/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Symbol
MYH9
NCBI Official Name
Myosin, heavy chain 9, non-muscle
NCBI Organism
Homo sapiens
Background Reference 01
Clark, K., (2008) J. Mol. Biol. 378 (4), 788-801.
Other Product Names
MYH9, DFNA17, EPSTS, FTNS, MGC104539, MHA, NMHC-II-A, NMMHCA, BDPLT6, NMMHC-IIA
Tested Applications
ELISA, WB
Protein ID
12667788
Physical Properties
Liquid
Curated Selection
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