AN301290L
Recombinant MYH9 Monoclonal Antibody
Size
£221.40
Was £246.00
- SKU:
- AN301290L
- Additional Names:
- MYH,DFNA,BDPLT,myosin,MYH9,BDPLT6,DFNA17,EPSTS,FTNS,MHA,NMHC-II-A,NMMHC-IIA,NMMHCA,myosin-9,heavy chain 9,myosin heavy chain 9,non-muscle,MYH9
- Application:
- IHC
- Concentration:
- 0.2 mg/ml
- Purification:
- Protein A Purified
- Storage Conditions:
- -20[o]C Avoid freeze/thaw cycles.
- Supplier:
- Elabscience
- Host:
- Rabbit
- Reactivities:
- Human, Mouse, Rat
- Buffer:
- PBS, 50% glycerol, 0.05% Proclin 300, 0.05% protein protectant.
- Immunogen:
- Recombinant Human MYH9 protein
- Clone:
- B1053
- Uniprot:
- P35579
- Synonyms:
- BDPLT6;cellular myosin heavy chain, type A;DFNA17;EPSTS;FTNS;MATINS;MHA;Myosin heavy chain 9;Myosin heavy chain, non-muscle IIa;myosin-9;myosin, heavy chain 9, non-muscle;NMHC-II-A;NMMHC-IIA;NMMHCA;non-muscle myosin heavy chain 9;non-muscle myosin heavy chain A;non-muscle myosin heavy chain IIa;non-muscle myosin heavy polypeptide 9;nonmuscle myosin heavy chain II-A
- Extra Details:
- 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.
- Shipping Conditions:
- Blue Ice