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AGL antibody
AGL
Reactivity: Human
ELISA, IHC
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-AGL Antibody
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Target
See all AGL Antibodies
AGL
(Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL))
Reactivity
All reactivities for AGL antibodies
Human
Host
All hosts for AGL antibodies
Rabbit
Clonality
All clonalities for AGL antibodies
Polyclonal
Conjugate
All conjugates for AGL antibodies
This AGL antibody is un-conjugated
Application
All applications for AGL antibodies
ELISA, Immunohistochemistry (IHC)
Characteristics
Polyclonal Antibody
Purification
Affinity purification
Immunogen
Synthetic peptide of human AGL
Isotype
IgG
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Alternatives
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Application Details
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Application Notes
IHC 1:25-1:100
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
0.2 mg/mL
Buffer
PBS with 0.05 % sodium azide and 50 % glycerol, PH7.4
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for AGL
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Target
AGL
(Amylo-alpha-1, 6-Glucosidase, 4-alpha-Glucanotransferase (AGL))
Alternative Name
AGL (AGL Products )
Synonyms
DDBDRAFT_0219237 antibody, DDBDRAFT_0234114 antibody, DDB_0219237 antibody, DDB_0234114 antibody, GDE antibody, 1110061O17Rik antibody, 9430004C13Rik antibody, 9630046L06Rik antibody, AI850929 antibody, C77197 antibody, amylo-alpha-1, 6-glucosidase, 4-alpha-glucanotransferase antibody, glycogen debranching enzyme antibody, glycogen debranching protein antibody, amylo-1,6-glucosidase, 4-alpha-glucanotransferase antibody, AGL antibody, agl antibody, MMAH_RS03870 antibody, Agl antibody
Background
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.
NCBI Accession
NP_000019
UniProt
P35573
Pathways
Cellular Glucan Metabolic Process
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