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Thermo Fisher Scientific PHKG2 Polyclonal Antibody
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Thermo Fisher Scientific PHKG2 Polyclonal Antibody

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Rabbit Polyclonal Antibody targeting human PHKG2. Validated for WB and ICC/IF. Recombinant protein immunogen. High specificity and affinity purified. Suitable for research use only.

카탈로그번호
PA584698
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 03:17
Thermo Fisher Scientific PA584698 PHKG2 Polyclonal Antibody 100 ul pk판매 단위 pk ·
재고 확인 필요
740,000원VAT 포함 814,000원

Thermo Fisher Scientific · Thermo Fisher Scientific PHKG2 Polyclonal Antibody

Applications

Western Blot (WB)

  • Tested Dilution: 0.04–0.4 µg/mL

Immunocytochemistry (ICC/IF)

  • Tested Dilution: 0.25–2 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Recombinant protein corresponding to Human PHKG2. Recombinant protein control fragment (Product #RP-105360)
Conjugate Unconjugated
Form Liquid
Concentration 0.1 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_2791849

Product Specific Information

Immunogen sequence:
LTAEQALQHP FFERCEGSQP WNLTPRQRFR VAVWTVLAAG RVALSTHRVR PLTKNALLRD PYALRSVRHL IDNCAFRLY


Target Information

PHKG2 is a testis/liver isoform of the phosphorylase kinase gamma subunit. Phosphorylase kinase is a polymer of 16 subunits, four each of alpha, beta, gamma, and delta. The alpha subunit includes skeletal muscle and hepatic isoforms encoded by two different genes. The beta subunit is common to both isoforms and encoded by one gene. The gamma subunit includes skeletal muscle and hepatic isoforms, with the hepatic isoform encoded by PHKG2. The delta subunit is a calmodulin encoded by three different genes. Gamma subunits contain the enzyme's active site, while alpha and beta subunits have regulatory functions controlled by phosphorylation. The delta subunit mediates calcium dependence. Mutations in PHKG2 cause glycogen storage disease type 9C (autosomal liver glycogenosis). Alternatively spliced transcript variants encoding different isoforms have been identified in PHKG2.


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

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