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Thermo Fisher Scientific PYGL Polyclonal Antibody
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Thermo Fisher Scientific PYGL Polyclonal Antibody

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Thermo Fisher Scientific의 PYGL Polyclonal Antibody는 인간, 마우스, 랫트 시료에 반응하며 Western blot, IHC, ICC, IP에 사용 가능합니다. 항원 친화 크로마토그래피로 정제된 고순도 항체로, PBS/glycerol 완충액에 보관됩니다. 연구용으로만 사용됩니다.

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마지막 업데이트 2025. 08. 05. 오전 10:51
Thermo Fisher Scientific PA576996 PYGL Polyclonal Antibody 100 ul pk판매 단위 pk ·
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731,200원VAT 포함 804,320원

Thermo Fisher Scientific · Thermo Fisher Scientific PYGL Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:2,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200
Immunocytochemistry (ICC/IF) 1:50–1:200
Immunoprecipitation (IP) 1:50–1:200

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant full length Human PYGL (UniProt ID: P06737-1, amino acids 1–847)
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 50% glycerol
Contains 0.02% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2720723

Product Specific Information

The antibody was affinity-purified from rabbit antiserum by affinity chromatography using an epitope-specific immunogen. The purity is greater than 95% as determined by SDS-PAGE.

Target Information

This gene encodes a homodimeric enzyme that catalyzes the cleavage of α-1,4-glucosidic bonds to release glucose-1-phosphate from liver glycogen stores. The enzyme is activated by phosphorylation at serine residue 15, switching from phosphorylase B to phosphorylase A. Its activity is regulated by allosteric effectors and hormonal control mechanisms.

Humans express three glycogen phosphorylase isozymes primarily in liver, brain, and muscle. The liver isozyme maintains systemic glucose levels, while the brain and muscle isozymes serve local energy demands. Mutations in the liver glycogen phosphorylase gene cause glycogen storage disease type VI (Hers disease), characterized by inhibited glycogen-to-glucose conversion, moderate hypoglycemia, mild ketosis, growth retardation, and hepatomegaly. Alternative splicing produces multiple transcript variants encoding different isoforms.


For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

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