A28325
MYH6/AA Alpha-MHC Rabbit monoclonal antibody

Size
POA
- SKU:
- A28325
- Additional Names:
- A830009F23Rik|alpha-MHC|alphaMHC|Myhc-a|Myhca
- Application:
- ELISA, WB, IHC-P, IF
- Molecular Weight:
- 250 kDa
- Species Reactivity:
- Mouse
- Purification:
- Affinity Purified
- Storage Conditions:
- -20[o]C Avoid freeze/thaw cycles.
- Supplier:
- Abclonal
- Host:
- Rabbit
- Reactivities:
- Mouse, Rat
- Immunogen:
- Synthetic peptide. This information is considered to be commercially sensitive.
- Formulation:
- Unmodified
- Sequence:
- LFSTYASADTGDSGKGKGGKKKGSSFQTVSALHRENLNKLMTNLKTTHPHFVRCIIPNERKAPGVMDNPLVMHQLRCNGVLEGIRICRKGFPNRILYGDF
- Uniprot:
- Q02566
- Synonyms:
- A830009F23Rik;AA517445;alph;alpha cardiac MHC;alpha myosin;alpha-MHC;alphaMHC;ASD3;cardiomyopathy, hypertrophic 1;CMD1EE;CMH14;MYHC;Myhc-;Myhc-a;myHC-alpha;MYHCA;myosin heavy chain 6;Myosin heavy chain, cardiac muscle alpha isoform;myosin heavy chain, cardiac muscle, adult;myosin-6;myosin, heavy polypeptide 6, cardiac muscle, alpha (cardiomyopathy, hypertrophic 1);SSS3
- Extra Details:
- Enables microfilament motor activity. Involved in cardiac muscle contraction. Acts upstream of or within several processes, including adult heart development; regulation of heart contraction; and striated muscle cell development. Located in Z disc and stress fiber. Part of myosin complex. Is expressed in several structures, including brown fat; embryo mesenchyme; great vessel of heart; heart; and skeletal musculature. Used to study dilated cardiomyopathy; dilated cardiomyopathy 1EE; and hypertrophic cardiomyopathy 14. Human ortholog(s) of this gene implicated in atrial heart septal defect (multiple); heart conduction disease (multiple); and intrinsic cardiomyopathy (multiple). Orthologous to human MYH6 (myosin heavy chain 6).
- Shipping Conditions:
- Blue Ice







