
Thermo Fisher Scientific MYH7 Monoclonal Antibody (TH81 (BGN/04/4481))
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Applications
Tested Dilution
Publications
Western Blot (WB)
1:4,000
View 1 publication 1 publication
Immunohistochemistry (Paraffin) (IHC (P))
Assay-dependent
Immunocytochemistry (ICC/IF)
Assay-dependent
ELISA (ELISA)
Assay-dependent
Product Specifications
Published species
Rat
Host/Isotype
Mouse / IgG1
Class
Monoclonal
Type
Antibody
Clone
TH81 (BGN/04/4481)
Immunogen
Myosin heavy chain from rabbit muscle. if (typeof window.$mangular === undefined
|| !window.$mangular) { window.$mangular = {}; } $mangular.antigenJson = \[{
targetFamily:
MYH7,
uniProtId:
P04461-1,
ncbiNodeId:
9986,
antigenRange:
1-736,
antigenLength:
736,
antigenImageFileName:
MA1-83347_MYH7_P04461-1_House_mouse.svg,
antigenImageFileNamePDP:
MA1-83347_MYH7_P04461-1_House_mouse_PDP.jpeg,
sortOrder:
3}\]
; $mangular.isB2BCMGT = false
; $mangular.isEpitopesModalImageMultiSizeEnabled = true
;
View immunogen .st0{fill:#FFFFFF;} .st1{fill:#1E8AE7;}
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
1 mg/mL
Storage conditions
Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_936651
Product Specific Information
Mouse anti Rabbit muscle myosin heavy chain antibody, clone TH81 recognizesthe heavy chain of rabbit muscle myosin.
Target Information
Muscle myosin is a hexameric protein containing 2 heavy chain subunits, 2 alkali light chain subunits, and 2 regulatory light chain subunits. This gene encodes the beta (or slow) heavy chain subunit of cardiac myosin. It is expressed predominantly in normal human ventricle. It is also expressed in skeletal muscle tissues rich in slow-twitch type I muscle fibers. Changes in the relative abundance of this protein and the alpha (or fast) heavy subunit of cardiac myosin correlate with the contractile velocity of cardiac muscle. Its expression is also altered during thyroid hormone depletion and hemodynamic overloading. Mutations in this gene are associated with familial hypertrophic cardiomyopathy, myosin storage myopathy, dilated cardiomyopathy, and Laing early-onset distal myopathy.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
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