catalog number :
MBS2506936
products type :
ELISA Kit
products full name :
Human CMLC-1 (Cardiac Myosin Light Chains 1) ELISA Kit
products short name :
[CMLC-1]
other names :
[cardiac myosin light chain-1; Myosin light chain 3; myosin light chain 3; CMLC1; cardiac myosin light chain 1; myosin light chain 1, slow-twitch muscle B/ventricular isoform; myosin, light polypeptide 3, alkali; ventricular, skeletal, slow; ventricular/slow twitch myosin alkali light chain; myosin, light chain 3, alkali; ventricular, skeletal, slow; Cardiac myosin light chain 1; CMLC1; Myosin light chain 1, slow-twitch muscle B/ventricular isoform; MLC1SB; Ventricular/slow twitch myosin alkali light chain]
products gene name :
[CMLC-1]
other gene names :
[MYL3; MYL3; CMH8; VLC1; MLC1V; MLC1SB; CMLC1; MLC1SB]
uniprot entry name :
MYL3_HUMAN
specificity :
This kit recognizes Human CMLC-1 in samples. No Significant cross-reactivity or interference between Human CMLC-1 and analogues was observed.
storage stability :
Store at 4 degree C.
image1 heading :
Typical Testing Data/Standard Curve (for reference only)
other info1 :
Samples: Serum, Plasma, Biological Fluids. Assay Type: Sandwich. Detection Range: 0.625-40ng/mL. Sensitivity: Min: 0.375ng/mL; Max: 40ng/mL
other info2 :
Intra-assay Precision: Intra-assay Precision (Precision within an assay): 3 samples with low, mid range and high level Human CMLC-1 were tested 20 times on one plate, respectively. Inter-assay Precision: Inter-assay Precision (Precision between assays): 3 samples with low, mid range and high level Human CMLC-1 were tested on 3 different plates, 20 replicates in each plate.
products description :
Intended Uses: This ELISA kit applies to the in vitro quantitative determination of Human CMLC-1 concentrations in serum, plasma and other biological fluids.
ncbi acc num :
AAF91089.1
ncbi mol weight :
21,932 Da
ncbi pathways :
Adrenergic Signaling In Cardiomyocytes Pathway (908257); Adrenergic Signaling In Cardiomyocytes Pathway (909696); Cardiac Muscle Contraction Pathway (93344); Cardiac Muscle Contraction Pathway (93992); Dilated Cardiomyopathy Pathway (121494); Dilated Cardiomyopathy Pathway (121285); Hypertrophic Cardiomyopathy (HCM) Pathway (114229); Hypertrophic Cardiomyopathy (HCM) Pathway (106591); Muscle Contraction Pathway (106261); Regulation Of Actin Cytoskeleton Pathway (198874)
ncbi summary :
MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy. [provided by RefSeq, Jul 2008]
uniprot summary :
MYL3: Regulatory light chain of myosin. Does not bind calcium. Defects in MYL3 are the cause of familial hypertrophic cardiomyopathy type 8 (CMH8). 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. CMH8 inheritance can be autosomal dominant or recessive. Protein type: Motor; Motility/polarity/chemotaxis. Chromosomal Location of Human Ortholog: 3p21.3-p21.2. Cellular Component: I band; sarcomere; muscle myosin complex; cytosol; A band. Molecular Function: actin monomer binding; structural constituent of muscle; motor activity; myosin II heavy chain binding; calcium ion binding. Biological Process: skeletal muscle development; metabolic process; positive regulation of ATPase activity; regulation of striated muscle contraction; ventricular cardiac muscle morphogenesis; regulation of the force of heart contraction; muscle filament sliding; cardiac muscle contraction. Disease: Cardiomyopathy, Familial Hypertrophic, 8
size5 :
10x96-Strip-Wells