Myosin Light Chain 3 (MYL3) Antibody

Product Graph
52€ (10 µg)

Por favor contáctenos para obtener información detallada sobre el precio y disponibilidad.

935106861
info@markelab.com
name
Myosin Light Chain 3 (MYL3) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx015098
tested applications
ELISA, WB

Description

Rabbit polyclonal antibody against MYL3 protein. Immunogen region is Internal.

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Primary Antibodies
Immunogen Target
Myosin Light Chain 3 (MYL3)
Host
Rabbit
Reactivity
Human
Recommended Dilution
WB: 1/500 - 1/3000, ELISA: 1/20000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified from rabbit antiserum by affinity chromatography using epitope-specific immunogen.
Size 1
10 µg
Size 2
100 µg
Size 3
200 µg
Size 4
300 µg
Size 5
1 mg
Form
Liquid
Tested Applications
ELISA, WB
Buffer
PBS (without Mg<sup>2+</sup> and Ca<sup>2+</sup>), pH 7.4, 150 mM NaCl, 0.02% sodium azide, 50% glycerol.
Availability
Shipped within 5-10 working days.
Storage
Aliquot and store at -20°C. Avoid repeated freeze/thaw cycles.
Dry Ice
No
UniProt ID
P08590
Background
Antibody anti-MYL3
Status
RUO
Note
Concentration: 1 mg/ml -

Descripción

Related Products

FNab05487

MYL3 antibody

Regulatory light chain of myosin. Does not bind calcium.

Ver Producto
FNab09860

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
abx005108

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