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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 및 개 시료에 반응하며, IHC(P) 실험에 적합합니다. 항원 친화 크로마토그래피로 정제된 액상 형태의 항체로, 1 mg/mL 농도이며 장기 보관 시 -20°C에서 안정적으로 유지됩니다. 연구용으로만 사용됩니다.

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pk
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마지막 업데이트 2025. 07. 27. 오후 04:12
Thermo Fisher Scientific PA533012 PYGL Polyclonal Antibody 50 ug pk판매 단위 pk
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700,900원VAT 포함 770,990원

Thermo Fisher Scientific · Thermo Fisher Scientific PYGL Polyclonal Antibody

Applications

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: 10 µg/mL
  • 참고: Heat-induced antigen retrieval in pH 6.0 citrate buffer 권장
  • 1차 항체 반응 후 biotinylated 2차 항체, alkaline phosphatase-streptavidin 및 chromogen 사용

Product Specifications

항목 내용
Species Reactivity Dog, Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic 10 amino acid peptide from internal region of human PYGL
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Antigen affinity chromatography
Storage buffer PBS
Contains 0.1% sodium azide
Storage conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping conditions Ambient (domestic); Wet ice (international)
RRID AB_2550473

Product Specific Information

  • Percent identity with other species by BLAST analysis:
    Human, Gorilla, Monkey, Dog (100%); Gibbon, Marmoset, Panda (90%); Mouse, Sheep, Hamster, Horse, Rabbit (80%)

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.
This protein switches from inactive phosphorylase B to active phosphorylase A by phosphorylation of serine residue 15.
Activity of this enzyme is regulated by allosteric effectors and hormonal controls.
Humans have three glycogen phosphorylase genes encoding distinct isozymes primarily expressed in liver, brain, and muscle.
The liver isozyme serves the glycemic demands of the body, while the brain and muscle isozymes supply those tissues.
In glycogen storage disease type VI (Hers disease), mutations inhibit glycogen conversion to glucose, resulting in 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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