MYH9 Rabbit Polyclonal Antibody (CAB16923)
- SKU:
- CAB16923
- Product Type:
- Antibody
- Reactivity:
- Human
- Mouse
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Antibody Type:
- Polyclonal Antibody
- Research Area:
- Cell Biology
Frequently bought together:
Description
Product Name: | MYH9 Rabbit Polyclonal Antibody |
SKU: | CAB16923 |
Size: | 20uL, 100uL |
Isotype: | IgG |
Host Species: | Rabbit |
Reactivity: | Human,Mouse,Rat |
Immunogen: | Recombinant fusion protein containing a sequence corresponding to amino acids 1801-1960 of human MYH9 (NP_002464.1). |
Sequence: | VKSK YKAS ITAL EAKI AQLE EQLD NETK ERQA ACKQ VRRT EKKL KDVL LQVD DERR NAEQ YKDQ ADKA STRL KQLK RQLE EAEE EAQR ANAS RRKL QREL EDAT ETAD AMNR EVSS LKNK LRRG DLPF VVPR RMAR KGAG DGSD EEVD GKAD GAEA KPAE |
Tested Applications: | WB IHC-P IF/ICC ELISA |
Recommended Dilution: | WB,1:100 - 1:500 IHC-P,1:50 - 1:200 IF/ICC,1:50 - 1:200 |
Synonyms: | MHA; FTNS; EPSTS; BDPLT6; DFNA17; MATINS; NMMHCA; NMHC-II-A; NMMHC-IIA; MYH9 |
Positive Sample: | HeLa,HT-29,A-549,NIH/3T3,C6 |
Cellular Localization: | Cytoplasm, cell cortex, cytoskeleton. |
Calculated MW: | 227kDa |
Observed MW: | 250kDa |
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.
Purification Method: | Affinity purification |
Gene ID: | 4627 |
Storage Buffer: | Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.01% thimerosal,50% glycerol,pH7.3. |