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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 PYGL 단백질을 인식하는 토끼 유래 IgG 항체로, WB, IHC, ICC/IF에 적합합니다. 항원 친화 크로마토그래피로 정제되었으며, PBS 기반의 안정적 저장용액을 제공합니다. 연구용으로만 사용 가능합니다.

카탈로그번호
PA552054
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 04:07
Thermo Fisher Scientific PA552054 PYGL Polyclonal Antibody 100 ul pk판매 단위 pk ·
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796,700원VAT 포함 876,370원

Thermo Fisher Scientific · Thermo Fisher Scientific PYGL Polyclonal Antibody

Applications

Application Tested Dilution Publications
Western Blot (WB) 0.04–0.4 µg/mL -
Immunohistochemistry (Paraffin) (IHC (P)) 1:200–1:500 -
Immunocytochemistry (ICC/IF) 0.25–2 µg/mL -

Product Specifications

Specification Description
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human PYGL (Product #RP-88882)
Conjugate Unconjugated
Form Liquid
Concentration 0.2 mg/mL
Purification Antigen affinity chromatography
Storage Buffer PBS, pH 7.2, with 40% 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_2646168

Product Specific Information

Immunogen sequence:
VVAATLQDII RRFKASKFGS TRGAGTVFDA FPDQVAIQLN DTHPALAIPE LMRIFVDIEK LPWSKAWELT QKTFAYTNHT VLPEALERWP VDLVEKLLPR HLEIIYEINQ KHLDRIVALF PKDVDRLRRM SLI

Antigen sequence identity to orthologs:

  • Mouse: 92%
  • Rat: 93%

Target Information

This gene encodes a homodimeric protein that catalyzes the cleavage of alpha-1,4-glucosidic bonds to release glucose-1-phosphate from liver glycogen stores. It switches from inactive phosphorylase B to active phosphorylase A by phosphorylation of serine residue 15. Activity is regulated by allosteric effectors and hormonal controls.

Humans have three glycogen phosphorylase genes expressed mainly in liver, brain, and muscle. The liver isozyme supports systemic glycemic demands, while the brain and muscle isozymes serve local tissues.

Mutations in the liver glycogen phosphorylase gene cause glycogen storage disease type VI (Hers disease), leading to moderate hypoglycemia, mild ketosis, growth retardation, and hepatomegaly. Alternative splicing results in 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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