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Thermo Fisher Scientific FGFR1 Monoclonal Antibody (OTI6F8), TrueMAB
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Thermo Fisher Scientific FGFR1 Monoclonal Antibody (OTI6F8), TrueMAB

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인간 FGFR1 단백질(aa 1-376)을 면역원으로 제작된 단클론 항체로, Western blot에 적합합니다. Mouse IgG2b 아이소타입이며, 동결건조 형태로 제공됩니다. PBS(8% 트레할로스) 완충액에 보관하며, -20°C에서 보존합니다. 연구용 전용 시약입니다.

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마지막 업데이트 2025. 08. 04. 오후 12:47
Thermo Fisher Scientific CF802989 FGFR1 Monoclonal Antibody (OTI6F8), TrueMAB 100 ug pk판매 단위 pk ·
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784,000원VAT 포함 862,400원

Thermo Fisher Scientific · Thermo Fisher Scientific FGFR1 Monoclonal Antibody (OTI6F8), TrueMAB

Applications

Western Blot (WB)

  • Tested Dilution: 1:2,000

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2b
Class Monoclonal
Type Antibody
Clone OTI6F8
Immunogen Human recombinant protein fragment corresponding to amino acids 1–376 of human FGFR1 produced in SF9 cell
Conjugate Unconjugated
Form Lyophilized
Concentration 1 mg/mL
Purification Affinity chromatography
Storage buffer PBS, pH 7.3, with 8% trehalose
Contains No preservative
Storage conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping conditions Ambient (domestic); Wet ice (international)

Product Specific Information

For reconstitution, add 100 µL of distilled water to obtain a final antibody concentration of approximately 1 mg/mL.
For conjugation experiments, perform an additional desalting step (e.g., Zeba Spin Desalting Columns, 7K MWCO, 0.5 mL, Product #89882).


Target Information

FGFR1 (also known as FLT2) is a member of the Fibroblast Growth Factor Receptor family (FGFR1–4), a group of membrane-spanning tyrosine kinases that act as high-affinity receptors for 17 growth factors (FGF1–17).
These receptors are involved in mesoderm induction, cell growth and migration, organ formation, and bone development.
FGFR1 undergoes alternative splicing, producing multiple variants expressed differently during embryonic and adult stages.
Mutations or aberrations in FGFR1 are associated with diseases such as Pfeiffer syndrome, idiopathic hypogonadotropic hypogonadism, Kallmann syndrome type 2, osteoglophonic dysplasia, and various craniofacial syndromes.
Chromosomal rearrangements involving FGFR1 are linked to stem cell myeloproliferative disorder and stem cell leukemia lymphoma syndrome.


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

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