dystrophia myotonica containing WD repeat motif Antibody

Novus Biologicals, part of Bio-Techne | Catalog # NBP2-49622

Novus Biologicals, part of Bio-Techne
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NBP2-49622
NBP2-49622-25ul
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Key Product Details

Species Reactivity

Validated:

Human

Predicted:

Mouse (94%), Rat (96%). Backed by our 100% Guarantee.

Applications

Immunohistochemistry, Immunohistochemistry-Paraffin

Label

Unconjugated

Antibody Source

Polyclonal Rabbit IgG

Concentration

Concentrations vary lot to lot. See vial label for concentration. If unlisted please contact technical services.

View all dystrophia myotonica containing WD repeat motif Antibodies »

Product Specifications

Immunogen

This antibody was developed against a recombinant protein corresponding to amino acids: TYLKWLPESESLFLASHASGHLYLYNVSHPCASAPPQYSLLKQGEGFSVYA

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Scientific Data Images for dystrophia myotonica containing WD repeat motif Antibody

Immunohistochemistry: dystrophia myotonica containing WD repeat motif Antibody [NBP2-49622]

Immunohistochemistry: dystrophia myotonica containing WD repeat motif Antibody [NBP2-49622]

Immunohistochemistry: dystrophia myotonica containing WD repeat motif Antibody [NBP2-49622] - Staining of human cerebral cortex shows positivity in neuronal processes.

Applications for dystrophia myotonica containing WD repeat motif Antibody

Application
Recommended Usage

Immunohistochemistry

1:500 - 1:1000

Immunohistochemistry-Paraffin

1:500 - 1:1000
Application Notes
For IHC-Paraffin, HIER pH 6 retrieval is recommended.

Formulation, Preparation, and Storage

Purification

Immunogen affinity purified

Formulation

PBS (pH 7.2) and 40% Glycerol

Preservative

0.02% Sodium Azide

Concentration

Concentrations vary lot to lot. See vial label for concentration. If unlisted please contact technical services.

Shipping

The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.

Stability & Storage

Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.

Background: dystrophia myotonica containing WD repeat motif

The gene that codes for DMWD (dystrophia myotonica WD-repeat containing protein) is located in the myotonic dystrophy (DM1) gene cluster on 19q. Mutations in the DM1 region affect DMPK (myotonic dystrophy protein kinase), a myosin kinase expressed in skeletal muscle, and are the cause of myotonic dystrophy, a form of muscular dystrophy characterized by wasting of the muscles and myotonia. DMWD is expressed ubiquitously and is most abundant in the testes and brain. Studies concerning its abundance and sub-cellular localization in brain tissue suggest that it may have a role in some of the mental symptoms associated with myotonic dystrophy. Alternate names for DMWD include DMR-N9, and DM9.

Alternate Names

D19S593E, DM9, DMRN9, DMR-N9, dystrophia myotonica WD repeat-containing protein, dystrophia myotonica, WD repeat containing, dystrophia myotonica-containing WD repeat motif, Dystrophia myotonica-containing WD repeat motif protein, gene59, Protein 59, Protein DMR-N9

Gene Symbol

DMWD

Additional dystrophia myotonica containing WD repeat motif Products

Product Documents for dystrophia myotonica containing WD repeat motif Antibody

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Certificate of Analysis

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Product Specific Notices for dystrophia myotonica containing WD repeat motif Antibody

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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