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PYGL Antibodies

AND PYGL ELISA kits, PYGL Proteins

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

We validate the specificity of these antibodies to PYGL by testing them on tissues known to express PYGL positively and negatively. Browse below to find the PYGL antibody that suites your experiment. We have 5 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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PYGL Infographic by Boster Bio

PYGL protein infographic

All PYGL Products

Filter by Application:

Product

Figures

Specificity

Applications

Price

Anti-PYGL Antibody

Human, Mouse, Rat

IP, IF, IHC, ICC, WB

$405
Cat # A06317
100ul

Human PYGL Recombinant Protein

SDS-PAGE

$268
Cat # PROTP06737
Starting from 10ug

Anti-PYGL Antibody (C-Term)

Human, Mouse

IHC-P, WB

$299
Cat # M06317
50 µl

PYGL (NM_002863) Human Over-expression Lysate

Human

$628
Cat # LS005836
100 µg

Anti-PYGL Antibody Picoband®

Human, Mouse, Rat

ELISA, Flow Cytometry, WB

$370
Cat # A06317-1
100 µg/vial

PYGL Overview

Facts about Glycogen phosphorylase, liver form.

PYGL 3D structure

PYGL 3D structure. Source: alphafold

Glycogen phosphorylase, liver form (PYGL)

Phosphorylase is an important allosteric enzyme in carbohydrate metabolism. Enzymes from different sources differ in their regulatory mechanisms and in their natural substrates.

However, all known phosphorylases share catalytic and structural properties. .

Gene Information

Human
Gene Name:	PYGL
Uniprot:	P06737
Entrez:	5836

Gene Information

Family

Belongs to:

glycogen phosphorylase family

Family

Alternative Names

EC 2.4.1.1; glycogen phosphorylase, liver form; GSD6; phosphorylase, glycogen, liver; phosphorylase, glycogen; liver

Molecular Weight

Mass (kDA):
97.149 kDA

Molecular Weight

Genomic Context


Human

Location:	14q22.1
Sequence:	14; NC_000014.9 (50905217..50944483, complement)

Diseases

Glycogen Storage Disease
Glycogen Storage Disease Type Vi
Hypoglycemia
Hepatomegaly
Storage Disease
Malignant Neoplasms
Neoplasms
Glycogen Storage Disease Type V
Cholangiocarcinoma
Diabetic Ketoacidosis
Mutation, Out-of-frame
Hypoxia
Glycogen Storage Disease Type Iv

Neoplasm, Residual
Fasting Hypoglycemia
Recurrent Severe Hypoglycemia
L1 Acute Lymphoblastic Leukemia
Neuroblastoma
Cell Transformation, Neoplastic
Hereditary Diseases

Disease

Interacting Proteins

PYGB

Interacting Proteins

Pathways

Localization
Transport
Stem Cell Differentiation
Response To Hypoxia
Metaphase
Neuron Differentiation
Oocyte Maturation
Oxidative Phosphorylation
Biosynthetic Process
Glucose Homeostasis
Senescence

Translation
Cell Cycle
Cell Differentiation
Cell Growth
Steroid Biosynthetic Process

Pathways

PTMs

Acetylation

Phosphoprotein

Research Areas

GPCR

Research Areas

Bosterbio | ELISA Kits, Antibodies, Antibody Company

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

References

PMID: 2877458 by Newgard C.B., et al. Sequence analysis of the cDNA encoding human liver glycogen phosphorylase reveals tissue-specific codon usage.

PMID: 9536091 by Chang S., et al. Identification of a mutation in liver glycogen phosphorylase in glycogen storage disease type VI.