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Western blot analysis of extracts of various cell lines, using MYH9 antibody (A16923) at 1:500 dilution.|Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.|Lysates/proteins: 25ug per lane.|Blocking buffer: 3% nonfat dry milk in TBST.|Detection: ECL Basic Kit (RM00020).|Exposure time: 1s.
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Immunohistochemistry of paraffin-embedded rat kidney using MYH9 Rabbit pAb (A16923) at dilution of 1:100 (40x lens).
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Immunohistochemistry of paraffin-embedded human thyroid cancer using MYH9 Rabbit pAb (A16923) at dilution of 1:100 (40x lens).
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Immunohistochemistry of paraffin-embedded human placenta using MYH9 Rabbit pAb (A16923) at dilution of 1:100 (40x lens).
MYH9 Rabbit pAb
Catalog No：AB-A16923
Manufacturer：ABclonal
Synonyms：MYH9;BDPLT6;DFNA17;EPSTS;FTNS;MHA;NMHC-II-A;NMMHC-IIA;NMMHCA;myosin-9
Applications：WB,IHC,IF
Reactivity：Human,Mouse,Rat
Host：Rabbit
Conjugate：No
€65,00 – €370,00
| Product Name: | MYH9 Rabbit pAb |
| Category: | Polyclonal Antibodies |
| Description: | 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. |
| Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 1711-1960 of human MYH9 (NP_002464.1). |
| Gene ID: | 4627 |
| Swiss prot: | P35579 |
| Molecular weight: | 159kDa/226kDa |
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