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Recombinant Human PYGL

CAT: 0013-GTR18893939-02Size: 100 µgDry Ice: NoHazardous: No
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CAT#:0013-GTR18893939-02Size:100 µg
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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Description
Recombinant Human PYGL
Product Name Alternative
Glycogen phosphorylase, Glycogen phosphorylase L, Glycogen phosphorylase liver, Glycogen phosphorylase liver form, GSD6, Hers disease, glycogen storage disease type VI, liver form, OTTHUMP00000233649, OTTHUMP00000233651, Phosphorylase glycogen liver, Pygl, PYGL_HUMAN
UniProt
P06737
Expression Region
745-847
Reactivity
Human
Tag
N-terminal His-IF2DI Tag
Source
E.Coli
Field of Research
Metabolism Research
Purity
Greater than 95% by SDS-PAGE gel analyses
Molecular Weight
32 KDa
Storage Conditions
-20°C for 12 months as lyophilized;2-8°C for 1 month under sterile conditions after reconstitution
Notes
For research use only.
Applications Notes
Centrifuge the vial at 10,000 rpm for 1 minute, reconstitute at 200 μg/ml in sterile distilled water by gentle pipetting 2-3 times, don’t vortex
Tested Applications
ELISA, WB
Preservative
Lyophilized from a 0.2 μm filtered solution in PBS with 5% trehalose, pH 7.4

UniProtKB · P06737

Glycogen phosphorylase, liver form

PYGL_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P06737
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
PYGL
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
2.4.1.1
Processing
—
Secondary accessions
A6NDQ4, B4DUB7, F5H816, O60567, O60752, O60913, Q501V9, Q641R5, Q96G82
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

PTM

AcetylationPhosphoprotein

Molecular function

Allosteric enzymeGlycosyltransferaseTransferase

Coding sequence diversity

Alternative splicing

Biological process

Carbohydrate metabolismGlycogen metabolism

Cellular component

Cytoplasm

Disease

Disease variantGlycogen storage disease

Ligand

Nucleotide-bindingPyridoxal phosphate

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