GeneTex
United States (US)

MYH3 antibody

GTX32147_3270_WB_20180221_18121410_750.jpg
GTX32147_1821_IHC-P_20180221_18121410_810.jpg

Cat No. GTX32147

Reference 2
Host Rabbit
Clonality Polyclonal
Isotype IgG
Application WB, IHC-P, ELISA
Reactivity Human, Mouse, Rat
See all MYH3 products
APPLICATION

Application Note

*Optimal dilutions/concentrations should be determined by the researcher.
Application Dilution
WB 1 μg/mL
IHC-P 5 μg/mL
ELISA Assay dependent
Not tested in other applications.

Calculated MW

224 kDa. ( Note )

Positive Control

Fetal Human Skeletal Muscle Lysate

Specificity/Sensitivity

MYH3 antibody is predicted to not cross-react with other members of the myosin heavy chain family.
PROPERTIES

Form

Liquid

Buffer

PBS with 0.02% sodium azide.

Storage

Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4ºC. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.

Concentration

1 mg/ml (Please refer to the vial label for the specific concentration.)

Antigen Species

Human

Immunogen

MYH3 antibody was raised against a 19 amino acid peptide near the amino terminus of human MYH3.The immunogen is located within amino acids 30 - 80 of MYH3.

Purification

Purified by antigen-affinity chromatography

Conjugation

Unconjugated

Note

For laboratory use only. Not for any clinical, therapeutic, or diagnostic use in humans or animals. Not for animal or human consumption.
TARGET

Synonyms

Myosin Heavy Chain 3,Da2A,Da2B,Da8,Hemhc,Myhc-Emb,Myhse1,Smhce,Myh3

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]

Database

Research Area

DATA IMAGES
GTX32147_3270_WB_20180221_18121410_750.jpg

GTX32147 WB Image

WB analysis of fetal human skeletal muscle lysate using GTX32147 MYH3 antibody.
Working concentration : 1 μg/ml
GTX32147_1821_IHC-P_20180221_18121410_810.jpg

GTX32147 IHC-P Image

IHC-P analysis of mouse skeletal muscle tissue using GTX32147 MYH3 antibody.
Working concentration : 5 μg/ml
REFERENCE

Application Reference

Zieba J et al. Sci Rep 2017; 7 : 41803 A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosis.
Application : IHC-P
Reactivity : Mouse
Zieba J et al. Sci Rep 2017; 7 : 41803 A postnatal role for embryonic myosin revealed by MYH3 mutations that alter TGFβ signaling and cause autosomal dominant spondylocarpotarsal synostosis.
Application : IHC-P
Reactivity : Mouse
Submit a Reference
Package List Price ($)
$ 339