Catalog No.
PHK55901
Species reactivity
Human
Host species
Rabbit
Isotype
IgG
Clonality
Polyclonal
Immunogen
E. coli - derived recombinant Human MYOT (Arg251-Thr441).
Tested applications
ELISA: 1:4000-1:8000, IHC: 1:50-1:100, WB: 1:1000-1:4000
Target
MYOT, 57 kDa cytoskeletal protein, TTID, Titin immunoglobulin domain protein, Myotilin, Myofibrillar titin-like Ig domains protein
Purification
Purified by antigen affinity column.
Accession
Q9UBF9
Applications
ELISA, IHC, WB
Form
Liquid
Storage buffer
0.01M PBS, pH 7.4, 50% Glycerol, 0.05% Proclin 300.
Stability and Storage
Use a manual defrost freezer and avoid repeated freeze thaw cycles. Store at 2 to 8°C for frequent use. Store at -20 to -80°C for twelve months from the date of receipt.
Solution structure of the first immunoglobulin domain of human myotilin., PMID:19418025
TAR DNA-Binding protein 43 accumulation in protein aggregate myopathies., PMID:19225410
Differential involvement of sarcomeric proteins in myofibrillar myopathies: a morphological and immunohistochemical study., PMID:19151983
In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathy., PMID:19050726
Electron microscopy in myofibrillar myopathies reveals clues to the mutated gene., PMID:18653338
Expression of mutant ubiquitin (UBB+1) and p62 in myotilinopathies and desminopathies., PMID:17931355
Beyond LGMD1A: myotilin is a component of central core lesions and nemaline rods., PMID:12899871
Myotilin, the limb-girdle muscular dystrophy 1A (LGMD1A) protein, cross-links actin filaments and controls sarcomere assembly., PMID:12499399
Indications for a novel muscular dystrophy pathway. gamma-filamin, the muscle-specific filamin isoform, interacts with myotilin., PMID:11038172
Myotilin, a novel sarcomeric protein with two Ig-like domains, is encoded by a candidate gene for limb-girdle muscular dystrophy., PMID:10369880