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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, 생쥐, 랫트 반응성을 가지며 Western blot, IHC, ICC/IF, ELISA, IP에 적합합니다. Rabbit IgG 기반 비결합 항체로, 고순도 친화 크로마토그래피로 정제되었습니다. -20°C에서 보관하며 연구용으로만 사용됩니다.

카탈로그번호
PA5110248
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 08:04
Thermo Fisher Scientific PA5110248 PYGL Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
627,600원VAT 포함 690,360원

Thermo Fisher Scientific · Thermo Fisher Scientific PYGL Polyclonal Antibody

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:1,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:50–1:200
Immunocytochemistry (ICC/IF) 1:50–1:200
ELISA 1 µg/mL
Immunoprecipitation (IP) 0.5 µg–4 µg antibody for 200 µg–400 µg extracts

Product Specifications

Property Description
Species Reactivity Human, Mouse, Rat
Host/Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant fusion protein containing a sequence corresponding to amino acids 690–847 of human PYGL (NP_0028543)
Conjugate Unconjugated
Form Liquid
Concentration 0.425 mg/mL
Purification Affinity Chromatography
Storage Buffer PBS, pH 7.3, with 50% glycerol
Contains 0.09% sodium azide
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Wet ice
RRID AB_2855659

Product Specific Information

Immunogen sequence:
IGTMDGANVE MAEEAGEENL FIFGMRIDDV AALDKKGYEA KEYYEALPEL KLVIDQIDNG FFSPKQPDLF KDIINMLFYH DRFKVFADYE AYVKCQDKVS QLYMNPKAWN TMVLKNIAAS GKFSSDRTIK EYAQNIWNVE PSDLKISLSN ESNKVNGN

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. The protein switches from inactive phosphorylase B to active phosphorylase A by phosphorylation at serine residue 15. Activity is regulated by allosteric effectors and hormonal controls. Humans have three glycogen phosphorylase genes expressed 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 produces multiple transcript variants.


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

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