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Thermo Fisher Scientific FGFR1 Monoclonal Antibody (2C1)
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Thermo Fisher Scientific FGFR1 Monoclonal Antibody (2C1)

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FGFR1 단백질을 표적으로 하는 Thermo Fisher Scientific의 Mouse Monoclonal Antibody (Clone 2C1). Western blot 및 ELISA에 적합하며, 인간 시료에 반응. 고순도 Affinity chromatography로 정제된 액상 형태로 제공되며, 연구용으로만 사용.

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마지막 업데이트 2025. 08. 05. 오후 10:24
Thermo Fisher Scientific H00002260-M17 FGFR1 Monoclonal Antibody (2C1) 100 ug pk판매 단위 pk ·
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518,100원VAT 포함 569,910원

Thermo Fisher Scientific · Thermo Fisher Scientific FGFR1 Monoclonal Antibody (2C1)

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 / IgG2a, kappa
Class Monoclonal
Type Antibody
Clone 2C1
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 (FGFR1–4), which serve as high-affinity receptors for 17 growth factors (FGF1–17).
The FGF receptor family plays a crucial role in various biological processes such as:

  • Mesoderm induction and patterning
  • Cell growth and migration
  • Organ formation and bone growth

FGFR1 is alternatively spliced, generating multiple splice variants expressed differently during embryonic development and in adult tissues. Mutations or defects in FGFR1 are associated with several diseases, 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 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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