
Thermo Fisher Scientific Aprutumab Recombinant Human Monoclonal Antibody
FGFR2를 표적으로 하는 인간 재조합 단일클론 항체로 ELISA 등 연구용에 적합. CHO 세포에서 발현된 IgG1 람다형 항체이며, Protein A로 정제됨. PBS(pH 7.5) 용액 형태, 방부제 무첨가. -20°C 이하에서 장기 보관 가능.
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Applications
- ELISA (ELISA): Assay-dependent
Product Specifications
| 항목 | 내용 |
|---|---|
| Species Reactivity | Human |
| Host / Isotype | Human / IgG1, lambda |
| Expression System | CHO cells |
| Class | Recombinant Monoclonal |
| Type | Antibody |
| Immunogen | Human FGFR2 |
| Conjugate | Unconjugated |
| Form | Liquid |
| Concentration | 2.9 mg/mL |
| Purification | Protein A |
| Storage Buffer | PBS, pH 7.5 |
| Contains | No preservative |
| Storage Conditions | -20°C, Avoid Freeze/Thaw Cycles |
| Shipping Conditions | Ambient (domestic); Wet ice (international) |
| RRID | AB_2911267 |
Product Specific Information
- Endotoxin level < 0.01 EU/µg by LAL method
- Use a manual defrost freezer and avoid repeated freeze-thaw cycles.
- Store at 2–8°C for one week.
- Store at -20 to -80°C for twelve months from the date of receipt.
Target Information
Aprutumab is a biosimilar that targets FGFR2.
FGFR2 is a member of the fibroblast growth factor receptor family and functions as a tyrosine-protein kinase receptor for fibroblast growth factors. It plays a key role in regulating cell proliferation, differentiation, migration, apoptosis, and embryonic development. FGFR family members differ in ligand affinities and tissue distribution.
Mutations in FGFR2 are associated with:
- Crouzon syndrome
- Pfeiffer syndrome
- Craniosynostosis
- Apert syndrome
- Jackson-Weiss syndrome
- Beare-Stevenson cutis gyrata syndrome
- Saethre-Chotzen syndrome
- Syndromic craniosynostosis
Multiple alternatively spliced transcript variants encoding different isoforms have been identified.
For Research Use Only.
Not for use in diagnostic procedures.
Not for resale without express authorization.
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