MYOM3 Polyclonal antibody

MYOM3 Polyclonal Antibody for IHC, IP, WB, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse, rat and More (1)

Applications

WB, IP, IHC, IF, ELISA

Conjugate

Unconjugated

Cat no : 17692-1-AP

Synonyms

MYOM3, Myomesin 3, Myomesin family member 3, myomesin family, member 3, RP11 293P20.1



Tested Applications

Positive WB detected inmouse skeletal muscle tissue, rat skeletal muscle tissue
Positive IP detected inmouse skeletal muscle tissue
Positive IHC detected inhuman skeletal muscle tissue, mouse skeletal muscle tissue
Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:500-1:3000
Immunoprecipitation (IP)IP : 0.5-4.0 ug for 1.0-3.0 mg of total protein lysate
Immunohistochemistry (IHC)IHC : 1:20-1:400
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Product Information

17692-1-AP targets MYOM3 in WB, IP, IHC, IF, ELISA applications and shows reactivity with human, mouse, rat samples.

Tested Reactivity human, mouse, rat
Cited Reactivityhuman, mouse, canine
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen MYOM3 fusion protein Ag11849
Full Name myomesin family, member 3
Calculated Molecular Weight 162 kDa, 136 kDa
Observed Molecular Weight 162 kDa
GenBank Accession NumberBC067101
Gene Symbol MYOM3
Gene ID (NCBI) 127294
RRIDAB_2146624
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen affinity purification
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA.

Background Information

MYOM3 (myomesin 3) is a structural component of the M-band in striated muscle and is involved in sarcomere stability and resistance during intense or sustained stretching. MYOM3 can be detected mainly in intermediate speed fibers of skeletal muscle. Recently high level of MYOM3 fragments were detected in sera from patients with muscular dystrophy, including Duchenne muscular dystrophy (DMD). MYOM3 fragments may be used as serum biomarker for DMD and other neuromuscular disorders. This antibody recognizes the intact MYOM3 protein (160-160 kDa) as well as MYOM3 fragments (100 kDa and 130 kDa). (26060189)

Protocols

Product Specific Protocols
WB protocol for MYOM3 antibody 17692-1-APDownload protocol
IHC protocol for MYOM3 antibody 17692-1-APDownload protocol
IP protocol for MYOM3 antibody 17692-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols

Publications

SpeciesApplicationTitle
mouseWB

J Clin Invest

A functional mini-GDE transgene corrects impairment in models of glycogen storage disease type III

Authors - Antoine Gardin
mouseWB

Nucleic Acids Res

Palmitic acid conjugation enhances potency of tricyclo-DNA splice switching oligonucleotides.

Authors - Karima Relizani
humanWB, IP

Hum Mol Genet

Serum proteomic profiling reveals fragments of MYOM3 as potential biomarkers for monitoring the outcome of therapeutic interventions in muscular dystrophies.

Authors - Jérémy Rouillon
mouseWB

Int J Mol Sci

Co-Administration of Simvastatin Does Not Potentiate the Benefit of Gene Therapy in the mdx Mouse Model for Duchenne Muscular Dystrophy.

Authors - Nathalie Bourg
humanIF

Stem Cell Reports

A Human Stem Cell Model of Fabry Disease Implicates LIMP-2 Accumulation in Cardiomyocyte Pathology.

Authors - Matthew J Birket
mouseWB

PLoS One

Mutant myocilin impacts sarcomere ultrastructure in mouse gastrocnemius muscle.

Authors - Jeffrey M Lynch