AGL (NM_000642) Human Mass Spec Standard

CAT#: PH310005

AGL MS Standard C13 and N15-labeled recombinant protein (NP_000633)


  View other "AGL" proteins (13)

USD 3,255.00

3 Weeks*

Size
    • 10 ug

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Frequently bought together (1)
Transient overexpression lysate of amylo-1, 6-glucosidase, 4-alpha-glucanotransferase (AGL), transcript variant 4
    • 100 ug

USD 436.00

Specifications

Product Data
Tag C-Myc/DDK
Species Human
Expression Host HEK293
Expression cDNA Clone or AA Sequence RC210005
Predicted MW 174.6 kDa
Protein Sequence
Purity > 80% as determined by SDS-PAGE and Coomassie blue staining
Concentration >0.05 µg/µL as determined by microplate BCA method
Labeling Method Labeled with [U- 13C6, 15N4]-L-Arginine and [U- 13C6, 15N2]-L-Lysine
Buffer 25 mM Tris-HCl, 100 mM glycine, pH 7.3
Storage Store at -80°C. Avoid repeated freeze-thaw cycles.
Stability Stable for 3 months from receipt of products under proper storage and handling conditions.
Reference Data
RefSeq NP_000633
RefSeq Size 7371
RefSeq ORF 4596
Synonyms GDE
Locus ID 178
UniProt ID P35573, A0A0S2A4E4
Cytogenetics 1p21.2
Summary This gene encodes the glycogen debrancher enzyme which is involved in glycogen degradation. This enzyme has two independent catalytic activities which occur at different sites on the protein: a 4-alpha-glucotransferase activity and a amylo-1,6-glucosidase activity. Mutations in this gene are associated with glycogen storage disease although a wide range of enzymatic and clinical variability occurs which may be due to tissue-specific alternative splicing. Alternatively spliced transcripts encoding different isoforms have been described. [provided by RefSeq, Jul 2008]
Protein Families Druggable Genome
Protein Pathways Metabolic pathways, Starch and sucrose metabolism

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