MYL3 antibody
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935106861
info@markelab.com
name
MYL3 antibody
category
Primary Antibodies
provider
FineTest
reference
FNab09860
tested applications
ELISA, WB, IF
Description
MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy.
Documents del producto
Product specifications
| Category | Primary Antibodies |
| Immunogen Target | MYL3 (MYL3) |
| Host | Rabbit |
| Reactivity | Human, Mouse, Rat |
| Recommended Dilution | WB: 1:500 - 1:2000; IF: 1:50 - 1:200 |
| Clonality | polyclonal |
| Conjugation | Unconjugated |
| Isotype | IgG |
| Observed MW | 23 kDa |
| Purity | ≥95% as determined by SDS-PAGE |
| Purification | Immunogen affinity purified |
| Size 1 | 100µg |
| Form | liquid |
| Tested Applications | ELISA, WB, IF |
| Storage | PBS with 0.02% sodium azide and 50% glycerol pH 7.3, -20℃ for 12 months(Avoid repeated freeze / thaw cycles.) |
| UniProt ID | P08590 |
| Gene ID | 4634 |
| Alias | Myosin light chain 3,Cardiac myosin light chain 1 (CMLC1),Myosin light chain 1, slow-twitch muscle B/ventricular isoform (MLC1SB),Ventricular myosin alkali light chain,Ventricular myosin light chain 1 (VLCl),Ventricular/slow twitch myosin alkali light chain (MLC-lV/sb),MYL3 |
| Background | Antibody anti-MYL3 |
| Status | RUO |
| Note | Mol. Weight 23 kDa |
Descripción
Related Products
MYL3 antibody
MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy.
Ver Producto
Myosin Light Chain 3 (MYL3) Antibody
MYL3 Antibody is a Rabbit Polyclonal antibody against MYL3. MYL3 encodes myosin light chain 3, an alkali light chain also referred to in the literature as both the ventricular isoform and the slow skeletal muscle isoform. Mutations in MYL3 have been identified as a cause of mid-left ventricular chamber type hypertrophic cardiomyopathy.
Ver Producto