
Thermo Fisher Scientific FGF23 Polyclonal Antibody, Biotin, PeproTech
인간 FGF-23 단백질을 검출하기 위한 Biotin 결합 폴리클로날 항체. Western blot 및 Sandwich ELISA에 최적화됨. 고순도 재조합 단백질로 면역한 토끼 유래 항체로 친화 크로마토그래피로 정제됨. 연구용으로만 사용 가능.
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Applications
Western Blot (WB)
- 사용 농도: 0.1–0.2 µg/mL
ELISA
- 사용 농도: 0.25–1.0 µg/mL
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Rabbit |
| Class | Polyclonal |
| Type | Antibody |
| Immunogen | E.coli-derived Recombinant Human FGF-23 (25.5 kDa) |
| Conjugate | Biotin |
| Form | Lyophilized |
| Purification | Affinity chromatography |
| Storage buffer | PBS |
| Contains | No preservative |
| Storage conditions | -20°C |
| Shipping conditions | Ambient |
Product Specific Information
Amino Acid Sequence of Recombinant Protein:
MYPNASPLLG SSWGGLIHLY TATARNSYHL QIHKNGHVDG APHQTIYSAL MIRSEDAGFV VITGVMSRRY LCMDFRGNIF GSHYFDPENC RFQHQTLENG YDVYHSPQYH FLVSLGRAKR AFLPGMNPPP YSQFLSRRNE IPLIHFNTPI PRRHTRSAED DSERDPLNVL KPRARMTPAP ASCSQELPSA EDNSPMASDP LGVVRGGRVN THAGGTGPEG CRPFAKFI
Preparation:
Produced from sera of rabbits immunized with highly pure Recombinant Human FGF-23. Anti-Human FGF-23-specific antibody was purified by affinity chromatography and then biotinylated.
Sandwich ELISA:
To detect Human FGF-23 by sandwich ELISA (using 100 µL/well), use 0.25–1.0 µg/mL of this antibody.
When used with PeproTech Polyclonal Anti-Human FGF-23 (500-P319) as a capture antibody, detection sensitivity is 2000–4000 pg/mL of Recombinant Human FGF-23.
Western Blot:
To detect Human FGF-23 by Western Blot, use 0.1–0.2 µg/mL.
Detection limit: 1.5–3.0 ng/lane (reducing or non-reducing conditions).
Package Information:
500-P319BT-1MG is provided as 2 × 500 µg.
Target Information
The FGF23 gene encodes a member of the fibroblast growth factor family, which has mitogenic and cell survival activities.
FGF family members are involved in embryonic development, cell growth, morphogenesis, tissue repair, tumor growth, and invasion.
FGF23 inhibits renal tubular phosphate transport and is associated with autosomal dominant hypophosphatemic rickets and oncogenic hypophosphatemic osteomalacia.
Mutations in this gene 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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