Myosin 9 antibody
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- Target See all Myosin 9 (MYH9) Antibodies
- Myosin 9 (MYH9)
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Reactivity
- Human, Mouse
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Host
- Rabbit
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Clonality
- Polyclonal
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Conjugate
- This Myosin 9 antibody is un-conjugated
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Application
- Western Blotting (WB), Immunohistochemistry (IHC)
- Purification
- Affinity purification
- Immunogen
- Recombinant protein of human MYH9
- Isotype
- IgG
- Top Product
- Discover our top product MYH9 Primary Antibody
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- Application Notes
- WB 1:1000 - 1:2000 IHC 1:50 - 1:100
- Restrictions
- For Research Use only
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- Concentration
- 1 mg/mL
- Buffer
- Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3.
- Preservative
- Sodium azide
- Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Storage
- -20 °C
- Storage Comment
- Store at -20°C. Avoid freeze / thaw cycles.
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- Target
- Myosin 9 (MYH9)
- Alternative Name
- MYH9 (MYH9 Products)
- Background
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Synonyms: BDPLT 6,BDPLT6,Cellular myosin heavy chain,Cellular myosin heavy chain type A,DFNA 17,DFNA17,EPSTS,FTNS,MGC104539,MHA,MYH 2A,MYH 9,MYH2A,MYH9,MYH9,MYHas8,MyHC 2A,MyHC IIa,MyHC2A,MyHCIIa,MYHSA 2,MYHSA2,Myosin 9,Myosin heavy chain 9,Myosin heavy chain 9 non muscle,Myosin heavy chain,Myosin heavy chain non muscle IIa,Myosin heavy chain nonmuscle IIa,Myosin heavy polypeptide 2,Myosin heavy polypeptide 9 non muscle,Myosin-9,Myosin9,NMHC II A,NMMHC A,NMMHC II a,NMMHC II-a,NMMHC IIA,NMMHC-A,NMMHC-IIA,NMMHCA,Non muscle myosin heavy chain A,Non muscle myosin heavy chain,Non muscle myosin heavy chain II A,Non muscle myosin heavy polypeptide 9,non-muscle IIa,Non-muscle myosin heavy chain A,Non-muscle myosin heavy chain IIa,Nonmuscle myosin heavy chain A,Nonmuscle myosin heavy chain II A,type A
Background: This gene encodes a conventional non-muscle myosin, this protein should not be confused with the unconventional myosin-9a or 9b (MYO9A or MYO9B). The encoded protein is a myosin IIA heavy chain that contains an IQ domain and a myosin head-like domain which is involved in several important functions, including cytokinesis, cell motility and maintenance of cell shape. Defects in this gene have been associated with non-syndromic sensorineural deafness autosomal dominant type 17, Epstein syndrome, Alport syndrome with macrothrombocytopenia, Sebastian syndrome, Fechtner syndrome and macrothrombocytopenia with progressive sensorineural deafness.
- Molecular Weight
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Observed_MW: 250kDa
Calculated_MW: 159kDa/226kDa
- Gene ID
- 4627
- UniProt
- P35579
- Pathways
- Regulation of G-Protein Coupled Receptor Protein Signaling, Integrin Complex
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