Typical Testing Data/Standard Curve (for reference only)
(Fig.1. Mouse Myosin heavy chain,MHC Standard Curve.)
Mouse Myosin Heavy Chain, MHC ELISA Kit | MHC elisa kit
Mouse Myosin Heavy Chain, MHC ELISA Kit
* Allow all reagents to warm to room temperature for at least 30 minutes before opening.
* Pre-rinse the pipet tip with reagent, use fresh pipet tips for each sample, standard and reagent to avoid contamination.
* Unused wells must be kept desiccated at 4 degree C in the sealed bag provided.
* Mix Thoroughly is very important for the result. It is recommended using low frequency oscillator or slight hand shaking every 10 minutes.
* It is recommended that all samples and standards be assayed in duplicate or triplicate.
Typical Testing Data/Standard Curve (for reference only)
(Fig.1. Mouse Myosin heavy chain,MHC Standard Curve.)
Typical Testing Data/Standard Curve (for reference only)
(Fig.1. Mouse Myosin heavy chain,MHC Standard Curve.)
Background: MYH7 (Myosin Heavy Chain 7) is a Protein Coding gene. Diseases associated with MYH7 include Liang Distal Myopathy and Scapuloperoneal Syndrome, Myopathic Type. Among its related pathways are Vesicle-mediated transport and Cardiac muscle contraction. GO annotations related to this gene include actin binding and calmodulin binding. An important paralog of this gene is MYH6.
NCBI and Uniprot Product Information
Uniprot Description
MYH7: Muscle contraction. Defects in MYH7 are the cause of familial hypertrophic cardiomyopathy type 1 (CMH1). Familial hypertrophic cardiomyopathy is a hereditary heart disorder characterized by ventricular hypertrophy, which is usually asymmetric and often involves the interventricular septum. The symptoms include dyspnea, syncope, collapse, palpitations, and chest pain. They can be readily provoked by exercise. The disorder has inter- and intrafamilial variability ranging from benign to malignant forms with high risk of cardiac failure and sudden cardiac death. Defects in MYH7 are the cause of myopathy myosin storage (MYOMS). In this disorder, muscle biopsy shows type 1 fiber predominance and increased interstitial fat and connective tissue. Inclusion bodies consisting of the beta cardiac myosin heavy chain are present in the majority of type 1 fibers, but not in type 2 fibers. Defects in MYH7 are the cause of scapuloperoneal myopathy MYH7-related (SPMM); also known as scapuloperoneal syndrome myopathic type. SPMM is a progressive muscular atrophia beginning in the lower legs and affecting the shoulder region earlier and more severely than distal arm. Defects in MYH7 are a cause of cardiomyopathy dilated type 1S (CMD1S). Dilated cardiomyopathy is a disorder characterized by ventricular dilation and impaired systolic function, resulting in congestive heart failure and arrhythmia. Patients are at risk of premature death. Defects in MYH7 are the cause of myopathy distal type 1 (MPD1). MPD1 is a muscular disorder characterized by early-onset selective weakness of the great toe and ankle dorsiflexors, followed by weakness of the finger extensors. Mild proximal weakness occasionally develops years later after the onset of the disease.
Protein type: Motility/polarity/chemotaxis; Motor
Chromosomal Location of Human Ortholog: 14 C3|14 28.01 cM
Cellular Component: cytoplasm; muscle myosin complex; myofibril; myosin complex; sarcomere; stress fiber; Z disc
Molecular Function: actin binding; actin-dependent ATPase activity; ATP binding; ATPase activity; calmodulin binding; microfilament motor activity; motor activity; nucleotide binding; protein heterodimerization activity; protein homodimerization activity
Biological Process: adult heart development; ATP metabolic process; cardiac muscle contraction; cardiac muscle hypertrophy in response to stress; muscle contraction; muscle filament sliding; regulation of heart rate; regulation of slow-twitch skeletal muscle fiber contraction; regulation of the force of heart contraction; regulation of the force of skeletal muscle contraction; skeletal muscle contraction; striated muscle contraction; transition between fast and slow fiber; ventricular cardiac muscle tissue morphogenesis
Research Articles on MHC
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Product Notes
The Mouse MHC myh7 (Catalog #AAA9718073) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA9718073 ELISA Kit recognizes Mouse MHC. It is sometimes possible for the material contained within the vial of "Myosin Heavy Chain, MHC, ELISA Kit" to become dispersed throughout the inside of the vial, particularly around the seal of said vial, during shipment and storage. We always suggest centrifuging these vials to consolidate all of the liquid away from the lid and to the bottom of the vial prior to opening. Please be advised that certain products may require dry ice for shipping and that, if this is the case, an additional dry ice fee may also be required.Precautions
All products in the AAA Biotech catalog are strictly for research-use only, and are absolutely not suitable for use in any sort of medical, therapeutic, prophylactic, in-vivo, or diagnostic capacity. By purchasing a product from AAA Biotech, you are explicitly certifying that said products will be properly tested and used in line with industry standard. AAA Biotech and its authorized distribution partners reserve the right to refuse to fulfill any order if we have any indication that a purchaser may be intending to use a product outside of our accepted criteria.Disclaimer
Though we do strive to guarantee the information represented in this datasheet, AAA Biotech cannot be held responsible for any oversights or imprecisions. AAA Biotech reserves the right to adjust any aspect of this datasheet at any time and without notice. It is the responsibility of the customer to inform AAA Biotech of any product performance issues observed or experienced within 30 days of receipt of said product. To see additional details on this or any of our other policies, please see our Terms & Conditions page.Item has been added to Shopping Cart
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