Mouse Myosin Binding Protein C, Slow Type (MYBPC1) ELISA Kit | MYBPC1 elisa kit
Mouse Myosin Binding Protein C, Slow Type (MYBPC1) ELISA Kit
No significant cross-reactivity or interference between Myosin Binding Protein C, Slow Type (MYBPC1) and analogues was observed.
To minimize extra influence on the performance, operation procedures and lab conditions, especially room temperature, air humidity, incubator temperature should be strictly controlled. It is also strongly suggested that the whole assay is performed by the same operator from the beginning to the end.
NCBI and Uniprot Product Information
NCBI Description
This gene encodes a member of the myosin-binding protein C family. Myosin-binding protein C family members are myosin-associated proteins found in the cross-bridge-bearing zone (C region) of A bands in striated muscle. The encoded protein is the slow skeletal muscle isoform of myosin-binding protein C and plays an important role in muscle contraction by recruiting muscle-type creatine kinase to myosin filaments. Mutations in this gene are associated with distal arthrogryposis type I. Alternatively spliced transcript variants encoding multiple isoforms have been observed for this gene. [provided by RefSeq, Dec 2011]
Uniprot Description
MYBPC1: Thick filament-associated protein located in the crossbridge region of vertebrate striated muscle a bands. In vitro it binds MHC, F-actin and native thin filaments, and modifies the activity of actin-activated myosin ATPase. It may modulate muscle contraction or may play a more structural role. Defects in MYBPC1 are the cause of arthrogryposis, distal, type 1B (DA1B). A form of distal arthrogryposis, a disease characterized by congenital joint contractures that mainly involve two or more distal parts of the limbs, in the absence of a primary neurological or muscle disease. Distal arthrogryposis type 1 is characterized largely by camptodactyly and clubfoot. Hypoplasia and/or absence of some interphalangeal creases is common. The shoulders and hips are less frequently affected. Defects in MYBPC1 may be a cause of autosomal recessive lethal congenital contractural syndrome (LCCS), a severe, neonatally lethal form of arthrogryposis. Belongs to the immunoglobulin superfamily. MyBP family. 3 isoforms of the human protein are produced by alternative splicing.
Protein type: Myosin-binding; Actin-binding
Chromosomal Location of Human Ortholog: 12q23.2
Cellular Component: myofibril; cytosol
Molecular Function: protein binding; structural constituent of muscle; titin binding; actin binding
Biological Process: cell adhesion; muscle filament sliding
Disease: Lethal Congenital Contracture Syndrome 4; Arthrogryposis, Distal, Type 1b
Research Articles on MYBPC1
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Product Notes
The Mouse MYBPC1 mybpc1 (Catalog #AAA2020793) is an ELISA Kit and is intended for research purposes only. The product is available for immediate purchase. The AAA2020793 ELISA Kit recognizes Mouse MYBPC1. It is sometimes possible for the material contained within the vial of "Myosin Binding Protein C, Slow Type (MYBPC1), 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
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