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Glycogen synthase 2 Antibody

Novus Biologicals, part of Bio-Techne | Catalog # NBP1-55133

Novus Biologicals, part of Bio-Techne
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NBP1-55133

Key Product Details

Species Reactivity

Human

Applications

Western Blot

Label

Unconjugated

Antibody Source

Polyclonal Rabbit IgG

Concentration

0.5 mg/ml

Product Specifications

Immunogen

Synthetic peptides corresponding to GYS2(glycogen synthase 2 (liver)) The peptide sequence was selected from the middle region of GYS2. Peptide sequence TLSRAFPDKFHVELTSPPTTEGFKYPRPSSVPPSPSGSQASSPQSSDVED. The peptide sequence for this immunogen was taken from within the described region.

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Theoretical MW

81 kDa.
Disclaimer note: The observed molecular weight of the protein may vary from the listed predicted molecular weight due to post translational modifications, post translation cleavages, relative charges, and other experimental factors.

Description

The addition of 50% glycerol is optional for those storing this antibody at -20C and not aliquoting smaller units. However, please note that glycerol may interrupt some downstream antibody applications and should be added with caution.

Scientific Data Images for Glycogen synthase 2 Antibody

Western Blot: Glycogen synthase 2 Antibody [NBP1-55133]

Western Blot: Glycogen synthase 2 Antibody [NBP1-55133]

Western Blot: Glycogen synthase 2 Antibody [NBP1-55133] - Human Muscle lysate, concentration 0.2-1 ug/ml.

Applications for Glycogen synthase 2 Antibody

Application
Recommended Usage

Western Blot

1.0 ug/ml

Formulation, Preparation, and Storage

Purification

Affinity purified

Formulation

PBS, 2% Sucrose

Preservative

0.09% Sodium Azide

Concentration

0.5 mg/ml

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: Glycogen synthase 2

GYS2 transfers the glycosyl residue from UDP-Glc to the non-reducing end of alpha-1,4-glucan. Defects in GYS2 are the cause of glycogen storage disease type 0 (GSD0).

Alternate Names

EC 2.4.1.11, glycogen [starch] synthase, liver, glycogen synthase 2 (liver)

Gene Symbol

GYS2

UniProt

Additional Glycogen synthase 2 Products

Product Documents for Glycogen synthase 2 Antibody

Certificate of Analysis

To download a Certificate of Analysis, please enter a lot number in the search box below.

Product Specific Notices for Glycogen synthase 2 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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