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Thermo Fisher Scientific FGF23 (Fibroblast Growth Factor 23) Monoclonal Antibody (FGF23/132)
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Thermo Fisher Scientific FGF23 (Fibroblast Growth Factor 23) Monoclonal Antibody (FGF23/132)

상품 한눈에 보기

인간 FGF23 단백질을 인식하는 마우스 단클론 항체로, IHC(P) 및 IHC(PFA) 실험에 적합합니다. Protein A/G 정제, PBS 기반 완충액에 보관되며 4°C에서 안정적입니다. 연구용으로만 사용 가능합니다.

카탈로그번호
8074-MSM30-Px (2개 옵션)
판매단위
pk
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2개 옵션
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마지막 업데이트 2025. 08. 04. 오후 05:32
Thermo Fisher Scientific 8074-MSM30-P1 FGF23 (Fibroblast Growth Factor 23) Monoclonal Antibody (FGF23/132) 100 ug pk판매 단위 pk ·
재고 확인 필요
900,300원VAT 포함 990,330원
Thermo Fisher Scientific 8074-MSM30-P0 FGF23 (Fibroblast Growth Factor 23) Monoclonal Antibody (FGF23/132) 20 ug pk판매 단위 pk ·
재고 확인 필요
449,700원VAT 포함 494,670원

Thermo Fisher Scientific · Thermo Fisher Scientific FGF23 (Fibroblast Growth Factor 23) Monoclonal Antibody (FGF23/132)

Applications and Tested Dilution

Application Tested Dilution
Immunohistochemistry (Paraffin) (IHC (P)) 2 µg/mL
Immunohistochemistry (PFA fixed) (IHC (PFA)) 1–2 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG
Class Monoclonal
Type Antibody
Clone FGF23/132
Immunogen Recombinant full-length human FGF23 protein
Conjugate Unconjugated
Form Liquid
Concentration 200 µg/mL
Purification Protein A/G
Storage Buffer PBS, pH 7.4, with 0.05% BSA
Contains 0.05% sodium azide
Storage Conditions 4°C, do not freeze
Shipping Conditions Ambient (domestic); Wet ice (international)

Target Information

The protein encoded by this gene is a member of the fibroblast growth factor (FGF) family. FGF family members have 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, an inherited phosphate-wasting disorder. Abnormally high expression has been observed in oncogenic hypophosphatemic osteomalacia, a disease characterized by abnormal phosphate metabolism. Mutations can also cause familial tumoral calcinosis with hyperphosphatemia.


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

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