PYGM Antibody (PACO16919)
제품 코드를 사용하여 Assay Genie 메인 사이트를 통해 주문합니다.
주문- SKU:
- PACO16919
- Product type:
- Antibody
- Reactivity:
- Human
- Reactivity:
- Mouse
- Reactivity:
- Rat
- Host Species:
- Rabbit
- Isotype:
- IgG
- Application:
- ELISA
- Application:
- WB
- Antibody type:
- Polyclonal
- Conjugation:
- Unconjugated
Frequently bought together:
Description
Antibody Name: | PYGM Antibody (PACO16919) |
Antibody SKU: | PACO16919 |
Size: | 50ul |
Host Species: | Rabbit |
Tested Applications: | ELISA, WB |
Recommended Dilutions: | ELISA:1:1000-1:2000, WB:1:200-1:1000 |
Species Reactivity: | Human, Mouse, Rat |
Immunogen: | Fusion protein of human PYGM |
Form: | Liquid |
Storage Buffer: | -20°C, pH7.4 PBS, 0.05% NaN3, 40% Glycerol |
Purification Method: | Antigen affinity purification |
Clonality: | Polyclonal |
Isotype: | IgG |
Conjugate: | Non-conjugated |
![]() | Gel: 8%SDS-PAGE, Lysate: 40 μg, Lane 1-3: Human fetal muscle tissue, mouse brain tissue, Mouse heart tissue, Primary antibody: PACO16919(PYGM Antibody) at dilution 1/450, Secondary antibody: Goat anti rabbit IgG at 1/8000 dilution, Exposure time: 40 seconds. |
Background: | This gene encodes a muscle enzyme involved in glycogenolysis. Highly similar enzymes encoded by different genes are found in liver and brain. Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency), a glycogen storage disease of muscle. Alternative splicing results in multiple transcript variants. |
Synonyms: | phosphorylase, glycogen, muscle |
UniProt Protein Function: | PYGM: 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. Dimers associate into a tetramer to form the enzymatically active phosphorylase A. Phosphorylation of Ser-14 converts phosphorylase B (unphosphorylated) to phosphorylase A. |
UniProt Protein Details: | Protein type:Transferase; Phosphorylase; Endoplasmic reticulum; Carbohydrate Metabolism - starch and sucrose; EC 2.4.1.1 Chromosomal Location of Human Ortholog: 11q12-q13.2 Cellular Component: cytoplasm; cytosol Molecular Function:protein binding; pyridoxal phosphate binding Biological Process: glycogen catabolic process; glycogen metabolic process Disease: Glycogen Storage Disease V |
NCBI Summary: | This gene encodes a muscle enzyme involved in glycogenolysis. Highly similar enzymes encoded by different genes are found in liver and brain. Mutations in this gene are associated with McArdle disease (myophosphorylase deficiency), a glycogen storage disease of muscle. Alternative splicing results in multiple transcript variants.[provided by RefSeq, Sep 2009] |
UniProt Code: | P11217 |
NCBI GenInfo Identifier: | 3041717 |
NCBI Gene ID: | 5837 |
NCBI Accession: | P11217.6 |
UniProt Secondary Accession: | P11217,A0AVK1, A6NDY6, |
UniProt Related Accession: | P11217 |
Molecular Weight: | 87,317 Da |
NCBI Full Name: | Glycogen phosphorylase, muscle form |
NCBI Synonym Full Names: | phosphorylase, glycogen, muscle |
NCBI Official Symbol: | PYGM |
NCBI Protein Information: | glycogen phosphorylase, muscle form |
UniProt Protein Name: | Glycogen phosphorylase, muscle form |
UniProt Synonym Protein Names: | Myophosphorylase |
Protein Family: | Glycogen phosphorylase |
UniProt Gene Name: | PYGM |
UniProt Entry Name: | PYGM_HUMAN |
Antibodies | ELISA Kits |
Anti-PYGM Antibody (CAB9392) | Human PYGM / Glycogen Phosphorylase, Muscle ELISA Kit |
Human Glycogen phosphorylase, muscle form (PYGM) ELISA Kit |
Secondary Antibody |
Anti-HRP Goat Anti-Rabbit IgG (H+L) Antibody (CABS014) |
Recommended Products |
Anti-FITC Goat Anti-Rabbit IgG (H+L) Antibody (CABS011) |
Anti-HRP-conjugated Beta Actin Antibody (CABC028) |