Recombinant Human COL6A2

Product Graph
Contáctenos para saber el precio

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

935106861
info@markelab.com
name
Recombinant Human COL6A2
category
Proteins and Peptides
provider
FineTest
reference
P4717
tested applications
Western Blot, ELISA

Documents del producto

Instrucciones
Data sheet
Descargar

Product specifications

Category
Proteins and Peptides
Host
E.Coli
Reactivity
Human
Assay Data
Centrifuge the vial before opening, reconstitute in sterile distilled water to a concentration of 0.1-1 mg/ml by gently pipetting 2-3 times, don't vortex.
Observed MW
24 kDa
Expression
820-1019
Purity
Greater than 90% as determined by SDS-PAGE.
Size 1
50μg
Size 2
200μg
Size 3
1mg
Form
Lyophilized powder
Tested Applications
Western Blot, ELISA
Buffer
Lyophilized from a 0.2 μm filtered solution in 10 mM Hepes, 500 mM NaCl with 5% trehalose, pH 7.4.
Availability
7 days
Storage
The lyophilized protein is stable at -20 °C for up to 1 year. After reconstitution, the protein solution is stable at -20 to -80 °C for 3 months or 1 week at 2 to 8 °C under sterile conditions. For extended storage, it is recommended to further dilute in working aliquots, avoid repeated freeze/thaw cycle.
UniProt ID
P12110
Alias
CO6A2_HUMAN, COL6A2, Collagen alpha 2(VI) chain, Collagen alpha-2(VI) chain, collagen type VI alpha 2, Collagen VI alpha 2 polypeptide, human mRNA for collagen VI alpha 2 C terminal globular domain, PP3610
Background
Protein COL6A2
Status
RUO
Note
Tag : N-terminal His Tag

Related Products

FNab01845

COL6A2 antibody

Ver Producto
P4717

Recombinant Human COL6A2

Ver Producto
abx002747

Collagen Type VI Alpha 2 (COL6A2) Antibody

COL6A2 Antibody is a Rabbit Polyclonal antibody against COL6A2. This gene encodes one of the three alpha chains of type VI collagen, a beaded filament collagen found in most connective tissues. The product of this gene contains several domains similar to von Willebrand Factor type A domains. These domains have been shown to bind extracellular matrix proteins, an interaction that explains the importance of this collagen in organizing matrix components. Mutations in this gene are associated with Bethlem myopathy and Ullrich scleroatonic muscular dystrophy. Three transcript variants have been identified for this gene.

Ver Producto