PIPA5114628

Phospho-PYGL (Ser15) Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA5114628-Each-of-1 In Stock ₹ 46,502.50

PIPA5114628 - Each of 1

₹ 46,502.50

In Stock

Quantity

1

Base Price: ₹ 46,502.50

GST (18%): ₹ 8,370.45

Total Price: ₹ 54,872.95

Antigen

Phospho-PYGL (Ser15)

Classification

Polyclonal

Conjugate

Unconjugated

Gene

PYGL

Gene Alias

glycogen liver; Glycogen phosphorylase, liver form; GPLL; GSD6; Lgp; liver glycogen phosphorylase; phosphorylase, glycogen, liver; PYGL

Host Species

Rabbit

Purification Method

sequential chromatography

Regulatory Status

RUO

Gene ID (Entrez)

110095, 5836, 64035

Content And Storage

-20°C

Form

Liquid

Applications

Immunohistochemistry (Paraffin), Western Blot

Concentration

1 mg/mL

Formulation

PBS with 50% glycerol and 0.02% sodium azide

Gene Accession No.

P06737, P09811, Q9ET01

Gene Symbols

PYGL

Immunogen

A synthesized peptide derived from human PYGL(Accession P06737), corresponding to amino acid residues around phosphorylated Ser17.

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse, Rat

Product Type

Antibody

Isotype

IgG

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Description

  • Antibody detects endogenous levels of PYGL only when phosphorylated at Ser15
  • This gene encodes a homodimeric protein that catalyses the cleavage of alpha-1,4-glucosidic bonds to release glucose-1-phosphate from liver glycogen stores
  • This protein switches from inactive phosphorylase B to active phosphorylase A by phosphorylation of serine residue 15
  • Activity of this enzyme is further regulated by multiple allosteric effectors and hormonal controls
  • Humans have three glycogen phosphorylase genes that encode distinct isozymes that are primarily expressed in liver, brain and muscle, respectively
  • The liver isozyme serves the glycemic demands of the body in general while the brain and muscle isozymes supply just those tissues
  • In glycogen storage disease type VI, also known as Hers disease, mutations in liver glycogen phosphorylase inhibit the conversion of glycogen to glucose and results in moderate hypoglycemia, mild ketosis, growth retardation and hepatomegaly
  • Alternative splicing results in multiple transcript variants encoding different isoforms.