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

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인간 PYGL 단백질을 인식하는 Thermo Fisher Scientific의 Rabbit Polyclonal Antibody. Western blot, IHC, ICC/IF 등 다양한 응용에 적합. 항원 친화 크로마토그래피로 정제되어 높은 특이성과 재현성을 제공. 연구용으로만 사용 가능.

카탈로그번호
PA551492
판매단위
pk
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마지막 업데이트 2025. 08. 01. 오후 07:04
Thermo Fisher Scientific PA551492 PYGL Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
799,600원VAT 포함 879,560원

Thermo Fisher Scientific · Thermo Fisher Scientific PYGL Polyclonal Antibody

Applications

Western Blot (WB)

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: 1:500–1:1,000
  • Publications: None

Immunocytochemistry (ICC/IF)

  • Tested Dilution: 0.25–2 µg/mL
  • Publications: None

Product Specifications

항목 내용
Species Reactivity Human
Published Species Not Applicable
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human PYGL (Product # RP-88883)
Conjugate Unconjugated
Form Liquid
Concentration 0.12 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, store at -20°C avoiding freeze/thaw cycles
Shipping Conditions Wet ice
RRID AB_2646167

Product Specific Information

Immunogen sequence:
MRIDDVAALD KKGYEAKEYY EALPELKLVI DQIDNGFFSP KQPDLFKDII NMLFYHDRFK VFADYEAYVK CQDKVSQLYM NPKAWNTMVL KNIAASGKFS SDRTIKEYAQ NIWNVEPSD

Antigen sequence identity:

  • Mouse: 94%
  • Rat: 92%

Target Information

This gene encodes a homodimeric protein that catalyzes the cleavage of α-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 for liver, brain, and muscle isozymes. The liver isozyme supports whole-body glycemic demands, while the brain and muscle isozymes serve localized needs. Mutations in liver glycogen phosphorylase cause glycogen storage disease type VI (Hers disease), leading to moderate hypoglycemia, mild ketosis, growth retardation, and hepatomegaly. Alternative splicing produces multiple transcript variants.


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

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