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GYS2 Antibodies

AND GYS2 ELISA kits, GYS2 Proteins

Many biological assays use antibodies to detect GYS2, such as Western Blot (WB), ELISA, Flow Cytometry, Immunocytochemistry (IHC). These antibodies can be polyclonal or monoclonal, and react with GYS2 in Human, Mouse, Rat, and many other animal samples. Boster Bio use mainly mouse and rabbit to develop GYS2 antibodies...

We validate the specificity of these antibodies to GYS2 by testing them on tissues known to express GYS2 positively and negatively. Browse below to find the GYS2 antibody that suites your experiment. We have 2 of these antibodies and many publications and validation images.

If you cannot find antibodies that fit your needs, contact us for making custom antibodies. We have a full suite of custom antibody services covering from research to diagnostic and therapeutic applications.

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GYS2 Infographic by Boster Bio

GYS2 protein infographic

All GYS2 Products

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Glycogen synthase 2 (GYS2) (NM_021957) Human Over-expression Lysate

Glycogen synthase 2 (GYS2) Human Over-expression Lysates NM_021957

Glycogen synthase 2 (GYS2) Human Over-expression Lysates NM_021957

Human

$960
Cat # LS002998
20 µg, 100 µg

Anti-GYS2 Antibody

boster box

Human, Mouse, Rat

ELISA, IP, IHC, WB

$370
Cat # A08086-1
100 μl/vial

GYS2 Overview

Facts about Glycogen [starch] synthase, liver.

GYS2 3D structure

GYS2 3D structure. Source: alphafold

Glycogen [starch] synthase, liver (GYS2)

Transfers the glycosyl residue from UDP-Glc to the non- reducing end of alpha-1,4-glucan. .

Gene Information

Human
Gene Name:	GYS2
Uniprot:	P54840
Entrez:	2998

Gene Information

Family

Belongs to:

glycosyltransferase 3 family

Family

Alternative Names

EC 2.4.1.11; glycogen [starch] synthase, liver; glycogen synthase 2 (liver)

Molecular Weight

Mass (kDA):
80.989 kDA

Molecular Weight

Genomic Context


Human

Location:	12p12.1
Sequence:	12; NC_000012.12 (21531527..21604858, complement)

Diseases

Glycogen Storage Disease
Hypoglycemia
Glycogen Synthase Deficiency
Fasting Hypoglycemia
Diabetes Mellitus
Hyperglycemia
Storage Disease
Obesity
Diabetes Mellitus, Non-insulin-dependent
Ketotic Hypoglycemia
Ketosis
Mood Disorders
Pediatric Obesity

Polycystic Ovary Syndrome
Parkinson Disease
Malignant Neoplasms
Gestational Diabetes
Dwarfism
Impaired Glucose Tolerance
Hypothyroidism

Disease

Pathways

Glucose Homeostasis
Gluconeogenesis
Transport
Circadian Rhythm
Pathogenesis
Secretion

Pathways

PTMs

Phosphorylation

Bosterbio | ELISA Kits, Antibodies, Antibody Company

For details, visit:
bosterbio.com/bosterbio-gene-info-cards/GYS2

References

PMID: 8203908 by Nuttall F.Q., et al. Primary structure of human liver glycogen synthase deduced by cDNA cloning.

PMID: 9691087 by Orho M., et al. Mutations in the liver glycogen synthase gene in children with hypoglycemia due to glycogen storage disease type 0.