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Glycogen Synthase 2 antibody (AA 594-703)
GYS2
Reactivity: Human
WB
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-Glycogen Synthase 2 Antibody
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Target
See all Glycogen Synthase 2 (GYS2) Antibodies
Glycogen Synthase 2 (GYS2)
(Glycogen Synthase 2, Liver (GYS2))
Binding Specificity
All epitopes for Glycogen Synthase 2 antibodies
AA 594-703
Reactivity
All reactivities for Glycogen Synthase 2 antibodies
Human
Host
All hosts for Glycogen Synthase 2 antibodies
Rabbit
Clonality
All clonalities for Glycogen Synthase 2 antibodies
Polyclonal
Conjugate
All conjugates for Glycogen Synthase 2 antibodies
This Glycogen Synthase 2 antibody is un-conjugated
Application
All applications for Glycogen Synthase 2 antibodies
Western Blotting (WB)
Sequence
DLLDWRYLGR YYQHARHLTL SRAFPDKFHV ELTSPPTTEG FKYPRPSSVP PSPSGSQASS PQSSDVEDEV EDERYDEEEE AERDRLNIKS PFSLSHVPHG KKKLHGEYKN
Cross-Reactivity
Mouse
Characteristics
Polyclonal Antibodies
Purification
Affinity purification
Immunogen
Recombinant fusion protein containing a sequence corresponding to amino acids 594-703 of human GYS2 (NP_068776.2).
Isotype
IgG
Top Product
Discover our top product GYS2 Primary Antibody
Alternatives
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Application Details
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Application Notes
WB,1:500 - 1:2000
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
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 Glycogen Synthase 2
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Target
Glycogen Synthase 2 (GYS2)
(Glycogen Synthase 2, Liver (GYS2))
Alternative Name
GYS2 (GYS2 Products )
Synonyms
cb765 antibody, zgc:112057 antibody, BC021322 antibody, LGS antibody, GLYSN antibody, glycogen synthase 2 antibody, gys2 antibody, Gys2 antibody, GYS2 antibody
Background
The protein encoded by this gene, liver glycogen synthase, catalyzes the rate-limiting step in the synthesis of glycogen - the transfer of a glucose molecule from UDP-glucose to a terminal branch of the glycogen molecule. Mutations in this gene cause glycogen storage disease type 0 (GSD-0) - a rare type of early childhood fasting hypoglycemia with decreased liver glycogen content.,GYS2,Cancer,Signal Transduction,PI3K-Akt Signaling Pathway,Cell Biology & Developmental Biology,Cytoskeleton,Actins,Endocrine & Metabolism,Carbohydrate metabolism,AMPK Signaling Pathway,Insulin Receptor Signaling Pathway,GYS2
Molecular Weight
80 kDa
Gene ID
2998
UniProt
P54840
Pathways
AMPK Signaling , Cellular Glucan Metabolic Process
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