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Glycogen Synthase 2 antibody
The Rabbit Polyclonal anti-Glycogen Synthase 2 antibody (ABIN7237113) specifically detects Glycogen Synthase 2 in ELISA and IHC.
The antibody is reactive with Human, Mouse and Rat samples.
Catalog No. ABIN7237113
$457.98
$538.80
save $80.82 (-15 %)
Plus shipping costs $50.00
20 μL ABIN7000693
60 μL ABIN7237111
120 μL ABIN7237112
200 μL ABIN7237113
20 μL ABIN7000693
60 μL ABIN7237111
120 μL ABIN7237112
200 μL ABIN7237113
Delivery in 11 to 14 Business Days
Quick Overview for Glycogen Synthase 2 antibody (ABIN7237113)
Target
See all Glycogen Synthase 2 (GYS2) Antibodies
Glycogen Synthase 2 (GYS2)
(Glycogen Synthase 2, Liver (GYS2))
Reactivity
All reactivities for Glycogen Synthase 2 antibodies
Human, Mouse, Rat
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
ELISA, Immunohistochemistry (IHC)
Product Details anti-Glycogen Synthase 2 Antibody
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Characteristics
Polyclonal Antibody
Purification
Affinity purification
Immunogen
Recombinant protein of human GYS2
Isotype
IgG
Alternatives
(show)
Application Details
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Application Notes
IHC 1:100-1:300
Restrictions
For Research Use only
Handling
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Format
Liquid
Concentration
0.3 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 Glycogen Synthase 2
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Target
Glycogen Synthase 2 (GYS2)
(Glycogen Synthase 2, Liver (GYS2))
Alternative Name
GYS2
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.
UniProt
P54840
Pathways
AMPK Signaling , Cellular Glucan Metabolic Process
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