ARG40487

anti-MYH3 antibody

anti-MYH3 antibody for IHC-Formalin-fixed paraffin-embedded sections,Western blot and Human,Mouse

Overview

Product Description Rabbit Polyclonal antibody recognizes MYH3
Tested Reactivity Hu, Ms
Tested Application IHC-P, WB
Specificity This antibody is human, mouse and rat reactive. The antibody is predicted to not cross-react with other members of the myosin heavy chain family.
Host Rabbit
Clonality Polyclonal
Isotype IgG
Target Name MYH3
Antigen Species Human
Immunogen 19 aa (N-terminus) of Human MYH3.
Conjugation Un-conjugated
Alternate Names Myosin heavy chain 3; MYHSE1; Myosin heavy chain, fast skeletal muscle, embryonic; Muscle embryonic myosin heavy chain; HEMHC; MYHC-EMB; Myosin-3; SMHCE

Application Instructions

Application Suggestion
Tested Application Dilution
IHC-P5 µg/ml
WB1 µg/ml
Application Note * The dilutions indicate recommended starting dilutions and the optimal dilutions or concentrations should be determined by the scientist.
Positive Control Jurkat

Properties

Form Liquid
Purification Affinity purification with immunogen.
Buffer PBS and 0.02% Sodium azide.
Preservative 0.02% Sodium azide
Concentration 1 mg/ml
Storage Instruction For continuous use, store undiluted antibody at 2-8°C for up to a week. For long-term storage, aliquot and store at -20°C or below. Storage in frost free freezers is not recommended. Avoid repeated freeze/thaw cycles. Suggest spin the vial prior to opening. The antibody solution should be gently mixed before use.
Note For laboratory research only, not for drug, diagnostic or other use.

Bioinformation

Database Links

GeneID: 17883 Mouse MYH3

GeneID: 4621 Human MYH3

Swiss-port # P11055 Human Myosin-3

Swiss-port # P13541 Mouse Myosin-3

Gene Symbol MYH3
Gene Full Name myosin, heavy chain 3, skeletal muscle, embryonic
Background Myosin is a major contractile protein which converts chemical energy into mechanical energy through the hydrolysis of ATP. Myosin is a hexameric protein composed of a pair of myosin heavy chains (MYH) and two pairs of nonidentical light chains. This gene is a member of the MYH family and encodes a protein with an IQ domain and a myosin head-like domain. Mutations in this gene have been associated with two congenital contracture (arthrogryposis) syndromes, Freeman-Sheldon syndrome and Sheldon-Hall syndrome. [provided by RefSeq, Jul 2008]
Function Muscle contraction. [UniProt]
Cellular Localization Cytoplasm, myofibril. Note=Thick filaments of the myofibrils. [UniProt]
Calculated MW 224 kDa