TPM3 antibody

Synonyms:CAPM1 antibody, CFTD antibody, HEL-189 antibody, HEL-S-82p antibody, hscp30 antibody, NEM1 antibody, OK/SW-cl.5 antibody, TM-5 antibody, TM3 antibody, TM30 antibody, TM30nm antibody, TM5 antibody, TPMsk3 antibody, TRK antibody
Catalogue No.:FNab08890Reactivity:Mouse
Host:RabbitTested Application:ELISA, WB, IHC
Clonality:polyclonalIsotype:IgG
  • SPECIFICATIONS
Product Name
TPM3 antibody
Catalogue No.
FNab08890
Size
100μg
Form
liquid
Purification
Immunogen affinity purified
Purity
≥95% as determined by SDS-PAGE
Clonality
polyclonal
Isotype
IgG
Storage
PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months (Avoid repeated freeze / thaw cycles.)
Immunogen
Immunogen
tropomyosin 3
Alternative Names
CAPM1 antibody, CFTD antibody, HEL-189 antibody, HEL-S-82p antibody, hscp30 antibody, NEM1 antibody, OK/SW-cl.5 antibody, TM-5 antibody, TM3 antibody, TM30 antibody, TM30nm antibody, TM5 antibody, TPMsk3 antibody, TRK antibody
UniProt ID
P06753
Observed MW
37 kDa
Application
Tested Applications
ELISA, WB, IHC
Recommended dilution
WB: 1:500 - 1:2000; IHC: 1:50 - 1:200
Validated Images
mouse skeletal muscle tissue were subjected to SDS PAGE followed by western blot with FNab08890(TPM3 antibody) at dilution of 1:1000
Immunohistochemistry of paraffin-embedded mouse heart using FNab08890(TPM3 antibody) at dilution of 1:50
Background
This gene encodes a member of the tropomyosin family of actin-binding proteins. Tropomyosins are dimers of coiled-coil proteins that provide stability to actin filaments and regulate access of other actin-binding proteins. Mutations in this gene result in autosomal dominant nemaline myopathy and other muscle disorders. This locus is involved in translocations with other loci, including anaplastic lymphoma receptor tyrosine kinase (ALK) and neurotrophic tyrosine kinase receptor type 1 (NTRK1), which result in the formation of fusion proteins that act as oncogenes. There are numerous pseudogenes for this gene on different chromosomes. Alternative splicing results in multiple transcript variants.