Collagen Type VI Alpha 2 (COL6A2) Antibody

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312€ (60 µl)

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935106861
info@markelab.com
name
Collagen Type VI Alpha 2 (COL6A2) Antibody
category
Primary Antibodies
provider
Abbexa
reference
abx002747
tested applications
WB

Description

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.

Documents del producto

Instrucciones
Data sheet
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Product specifications

Category
Primary Antibodies
Immunogen Target
Collagen Type VI Alpha 2 (COL6A2)
Host
Rabbit
Reactivity
Human, Mouse
Recommended Dilution
WB: 1/200 - 1/2000. Optimal dilutions/concentrations should be determined by the end user.
Clonality
Polyclonal
Conjugation
Unconjugated
Isotype
IgG
Purification
Purified by affinity chromatography.
Size 1
60 µl
Size 2
120 µl
Size 3
200 µl
Form
Liquid
Tested Applications
WB
Buffer
PBS, pH 7.3, containing 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
P12110
Gene ID
1292
NCBI Accession
NP_001840.3
Background
Antibody anti-COL6A2
Status
RUO
Note
Concentration: 1 mg/ml -

Descripción

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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