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Thermo Fisher Scientific Glypican 3 Monoclonal Antibody (GT2473)
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Thermo Fisher Scientific Glypican 3 Monoclonal Antibody (GT2473)

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인간 Glypican-3 단백질을 인식하는 Mouse IgG1 단일클론 항체로, WB, IHC, ICC/IF에 적합합니다. HepG2 세포를 양성 대조군으로 사용하며, Protein G 정제, PBS/glycerol 저장 buffer 구성. 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 08. 05. 오전 05:36
Thermo Fisher Scientific MA531552 Glypican 3 Monoclonal Antibody (GT2473) 100 ul pk판매 단위 pk ·
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657,900원VAT 포함 723,690원

Thermo Fisher Scientific · Thermo Fisher Scientific Glypican 3 Monoclonal Antibody (GT2473)

Applications

Application Tested Dilution
Western Blot (WB) 1:500–1:3,000
Immunohistochemistry (Paraffin) (IHC (P)) 1:100–1:1,000
Immunocytochemistry (ICC/IF) 1:100–1:1,000

Product Specifications

Specification Description
Species Reactivity Human
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Clone GT2473
Immunogen Recombinant protein encompassing a sequence within the C-terminus region of human Glypican-3
Conjugate Unconjugated
Form Liquid
Concentration 0.4 mg/mL
Purification Protein G
Storage Buffer PBS, pH 7, with 20% glycerol
Contains No preservative
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_2787180

Product Specific Information

  • Keep as concentrated solution.
  • Predicted reactivity: Chimpanzee (96%), Bovine (81%).
  • Positive Control: HepG2, HepG2 (24 µg/mL Tunicamycin treatment for 16 hr).
  • Centrifuge briefly prior to opening the vial.
  • Store product as a concentrated solution.

Target Information

GPC3 is a cell surface proteoglycan that bears heparan sulfate. This protein may be involved in the suppression or modulation of growth in predominantly mesodermal tissues and organs, and may play a role in the modulation of IGF2 interactions with its receptor. Members of the glypican-related integral membrane proteoglycan family contain a core protein anchored to the cytoplasmic membrane via a glycosyl phosphatidylinositol (GPI) linkage. These proteins may play a role in cell division control, growth regulation, and tumor predisposition. Deletion mutations in GPC3 cause Simpson-Golabi-Behmel syndrome (SGBS), characterized by pre- and postnatal overgrowth with visceral and skeletal anomalies.

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

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