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Thermo Fisher Scientific FGF23 (Fibroblast Growth Factor 23) Monoclonal Antibody (FGF23, 4168)
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Thermo Fisher Scientific FGF23 (Fibroblast Growth Factor 23) Monoclonal Antibody (FGF23, 4168)

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FGF23 단백질을 인식하는 마우스 단일클론 항체로 인간 시료에 반응합니다. IHC(P) 및 Peptide Array에 사용 가능하며, 고순도의 Protein A/G 정제 항체입니다. 보존제가 없는 액상 형태로 -20°C 이하에서 보관합니다.

카탈로그번호
8074-MSM8-P1ABX
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 05:33
Thermo Fisher Scientific 8074-MSM8-P1ABX FGF23 (Fibroblast Growth Factor 23) Monoclonal Antibody (FGF23, 4168) 100 ug pk판매 단위 pk ·
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825,100원VAT 포함 907,610원

Thermo Fisher Scientific · Thermo Fisher Scientific FGF23 (Fibroblast Growth Factor 23) Monoclonal Antibody (FGF23, 4168)

Applications

Immunohistochemistry (Paraffin) (IHC (P))

  • Tested Dilution: 1–2 µg/mL

Peptide Array (Array)

  • Tested Dilution: Assay-dependent

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2c, kappa
Class Monoclonal
Type Antibody
Clone FGF23, 4168
Immunogen Recombinant fragment (around aa25–251) of human FGF23 protein
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A/G
Storage Buffer PBS, pH 7.4
Contains No preservative
Storage Conditions -20°C or -80°C if preferred
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

  • For immunohistochemistry (PFA fixed): incubate antibody for 30 minutes at room temperature.
  • For staining of formalin-fixed tissues: heat tissue sections in 10 mM Tris with 1 mM EDTA, pH 9.0, for 45 minutes at 95°C, followed by cooling at room temperature for 20 minutes.

Target Information

The protein encoded by this gene is a member of the fibroblast growth factor family. FGF family members possess broad mitogenic and cell survival activities and are involved in various biological processes including embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion. The product of this gene inhibits renal tubular phosphate transport.
Mutations in this gene are associated with autosomal dominant hypophosphatemic rickets and familial tumoral calcinosis with hyperphosphatemia. Abnormally high expression levels have been found in oncogenic hypophosphatemic osteomalacia, a disease caused by abnormal phosphate metabolism.


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

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