LYAG/GAA Antibody (5L2L10)

Novus Biologicals, part of Bio-Techne | Catalog # NBP3-15698

Recombinant Monoclonal Antibody
Novus Biologicals, part of Bio-Techne
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NBP3-15698-100ul
NBP3-15698-20ul
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Key Product Details

Species Reactivity

Human

Applications

Western Blot

Label

Unconjugated

Antibody Source

Recombinant Monoclonal Rabbit IgG Clone # 5L2L10

Concentration

Please see the vial label for concentration. If unlisted please contact technical services.

View all Lysosomal alpha-Glucosidase Antibodies »

Product Specifications

Immunogen

A synthetic peptide corresponding to a sequence within amino acids 100-200 of human LYAG/GAA (P10253). QEQCEARGCCYIPAKQGLQGAQMGQPWCFFPPSYPSYKLENLSSSEMGYTATLTRTTPTFFPKDILTLRLDVMMETENRLHFTIKDPANRRYEVPLETPHV

Clonality

Monoclonal

Host

Rabbit

Isotype

IgG

Scientific Data Images for LYAG/GAA Antibody (5L2L10)

Western Blot: LYAG/GAA Antibody (5L2L10) [NBP3-15698]

Western Blot: LYAG/GAA Antibody (5L2L10) [NBP3-15698]

Western Blot: LYAG/GAA Antibody (5L2L10) [NBP3-15698] - Western blot analysis of extracts of various cell lines, using LYAG/GAA antibody (NBP3-15698) at 1:1000 dilution. Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) at 1:10000 dilution. Lysates/proteins: 25ug per lane. Blocking buffer: 3% nonfat dry milk in TBST. Detection: ECL Basic Kit. Exposure time: 10s.

Applications for LYAG/GAA Antibody (5L2L10)

Application
Recommended Usage

Western Blot

1:500 - 1:1000

Formulation, Preparation, and Storage

Purification

Affinity purified

Formulation

PBS, 0.05% BSA, 50% glycerol, pH7.3

Preservative

0.02% Sodium Azide

Concentration

Please see the 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 -20C. Avoid freeze-thaw cycles.

Background: Lysosomal alpha-Glucosidase

GAA encodes acid alpha-glucosidase, which is essential for the degradation of glycogen to glucose in lysosomes. Different forms of acid alpha-glucosidase are obtained by proteolytic processing. Defects in this gene are the cause of glycogen storage disease II, also known as Pompe's disease, which is an autosomal recessive disorder with a broad clinical spectrum. Three transcript variants encoding the same protein have been found for this gene. [provided by RefSeq]

Long Name

Glucosidase, Alpha; Acid

Alternate Names

Acid alpha-Glucosidase, Acid Maltase, GAA, LYAG, Lysosomal alphaGlucosidase

Gene Symbol

GAA

Additional Lysosomal alpha-Glucosidase Products

Product Documents for LYAG/GAA Antibody (5L2L10)

Product Datasheets

Certificate of Analysis

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

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Product Specific Notices for LYAG/GAA Antibody (5L2L10)

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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