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AGL Antibody

CAT: 0864-A52240-100ULSize: 100 µLDry Ice: NoHazardous: No
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CAT#:0864-A52240-100ULSize:100 µL
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24/48H Stock Items & 2 to 6 Weeks non Stock Items.
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CAS Number
9007-83-4
Gene Aliases
1110061O17Rik, 4-1, 4-glucantransferase, 6-glucosidase, 9430004C13Rik, 9630046L06Rik, AGL, AI850929, Amylo 1 6 glucosidase 4 alpha glucanotransferase, Amylo-1, Amylo-alpha-1, C77197, Dextrin 6-alpha-D-glucosidase, GDE, GDE_HUMAN, Glycogen debrancher, Glycogen debranching enzyme, Glycogen storage disease type III, Oligo-1
UniProt
P35573
Host
Rabbit
Antigen Species
Human
Reactivity
Human
Target Antigen
Synthetic peptide of Human AGL
Target
AGL
Clonality
Polyclonal
Conjugation
Non-conjugated
Applications
ELISA, IHC, ELISA:1:2000-1:5000, IHC:1:25-1:100
Field of Research
Signal Transduction
Purification Method
Antigen affinity purified
Form
Liquid
Buffer
PBS, 0.05% sodium azide, 40% glycerol, pH 7.4.
Storage Conditions
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Fragment
IgG

UniProtKB · P35573

Glycogen debranching enzyme

GDE_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P35573
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
AGL
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
A6NCX7, A6NEK2, D3DT51, P78354, P78544, Q59H92, Q6AZ90, Q9UF08
Protein keywords

Technical term

3D-structureDirect protein sequencingProteomics identificationReference proteome

Coding sequence diversity

Alternative splicing

Cellular component

Cytoplasm

Disease

Disease variantGlycogen storage disease

Biological process

Glycogen biosynthesis

Molecular function

GlycosidaseGlycosyltransferaseHydrolaseMultifunctional enzymeTransferase

PTM

PhosphoproteinUbl conjugation

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