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Thermo Fisher Scientific FGFR1 Monoclonal Antibody (2F7)
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Thermo Fisher Scientific FGFR1 Monoclonal Antibody (2F7)

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FGFR1 단백질을 인식하는 Thermo Fisher Scientific의 단클론 항체(2F7)로, 인간 시료에 반응하며 Western blot과 ELISA에 적합합니다. 비결합형 액상 형태로, PBS 버퍼에 보존되며 -20°C에서 보관합니다. 연구용으로만 사용 가능합니다.

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마지막 업데이트 2025. 08. 04. 오후 08:00
Thermo Fisher Scientific H00002260-M06 FGFR1 Monoclonal Antibody (2F7) 100 ug pk판매 단위 pk ·
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518,100원VAT 포함 569,910원

Thermo Fisher Scientific · Thermo Fisher Scientific FGFR1 Monoclonal Antibody (2F7)

Applications

Western Blot (WB)

  • Tested Dilution: 1–5 µg/mL

ELISA

  • Tested Dilution: 10 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2b, kappa
Class Monoclonal
Type Antibody
Clone 2F7
Immunogen FGFR1 (NP_000595.1, 303–408 a.a.) partial recombinant protein with GST tag (MW of GST tag alone: 26 kDa)
Conjugate Unconjugated
Form Liquid
Concentration See Label
Purification Affinity chromatography
Storage Buffer PBS, pH 7.4
Contains No preservative
Storage Conditions -20°C, Avoid Freeze/Thaw Cycles
Shipping Conditions Ambient (domestic); Wet ice (international)

Product Specific Information

Sequence of this protein is as follows:
DNLPYVQILK TAGVNTTDKE MEVLHLRNVS FEDAGEYTCL AGNSIGLSHH SAWLTVLEAL EERPAVMTSP LYLEIIIYCT GAFLISCMVG SVIVYKMKSG TKKSDF


Target Information

FGFR1 (also known as FLT2) is a member of the Fibroblast Growth Factor Receptor family, consisting of four membrane-spanning tyrosine kinases (FGFR1–4). These receptors serve as high-affinity binding sites for 17 growth factors (FGF1–17). The FGF receptor family is crucial in various biological processes such as mesoderm induction, cell growth and migration, organ formation, and bone development.
FGFR1 undergoes alternative splicing, resulting in multiple variants expressed differently during embryonic development and in adult tissues.
Mutations or defects in FGFR1 are linked to several disorders, including:

  • Pfeiffer syndrome (PS)
  • Idiopathic hypogonadotropic hypogonadism (IHH)
  • Kallmann syndrome type 2 (KAL2)
  • Osteoglophonic dysplasia (OGD)
  • Non-syndromic trigonocephaly
  • Jackson-Weiss syndrome
  • Antley-Bixler syndrome

Chromosomal aberrations involving FGFR1 are associated with 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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