adult 2 antibody
Fast 2a myosin heavy chain antibody
IBM3 antibody
Inclusion body myopathy 3, autosomal dominant antibody
MYH2 antibody
MYH2_HUMAN antibody
MYH2A antibody
MYHas8 antibody
MyHC IIa antibody
MyHC-2a antibody
MyHC-IIa antibody
MYHSA2 antibody
Myosin heavy chain 2 antibody
Myosin heavy chain 2a antibody
Myosin heavy chain antibody
Myosin heavy chain IIa antibody
Myosin heavy chain skeletal muscle adult 2 antibody
Myosin heavy polypeptide 2 skeletal muscle adult antibody
Myosin-2 antibody
MYPOP antibody
skeletal muscle antibody
Type IIA myosin heavy chain antibody
Concentration:
1 mg/ml
Clonality:
Recombinant
Conjugation:
Non-conjugated
Price:
Consultar
Format:
Liquid
Immunogen:
Synthetic peptide within Human MYH2 aa 50-150.
Host:
Rabbit
Reactivity:
Human, Mouse, Rat
Application:
WB,IHC-P
Description:
Defects in MYH2 are the cause of inclusion body myopathy type 3 (IBM3) [MIM:605637]. Hereditary inclusion body myopathies constitute a group of neuromuscular disorders characterized by slowly progressive distal and proximal weakness and a typical muscle p
Cell localization:
Cytoplasm.
Isotype:
IgG
Positive control:
Mouse skeletal muscle tissue lysate, rat skeletal muscle tissue lysate, human skeletal muscle tissue, mouse skeletal muscle tissue, rat skeletal muscle tissue.
Storage conditions:
Store at +4? after thawing. Aliquot store at -20?. Avoid repeated freeze / thaw cycles.
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