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Thermo Fisher Scientific FGFR1 Monoclonal Antibody (3B2)
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Thermo Fisher Scientific FGFR1 Monoclonal Antibody (3B2)

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FGFR1 단백질을 인식하는 Mouse monoclonal antibody (Clone 3B2). Western blot 및 ELISA에 적합하며, 인간 시료에 반응. PBS 용액 내 보관, 보존제 없음. 연구용으로 세포 신호전달 및 성장 관련 연구에 활용 가능.

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마지막 업데이트 2025. 08. 04. 오후 08:00
Thermo Fisher Scientific H00002260-M13 FGFR1 Monoclonal Antibody (3B2) 100 ug pk판매 단위 pk ·
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518,100원VAT 포함 569,910원

Thermo Fisher Scientific · Thermo Fisher Scientific FGFR1 Monoclonal Antibody (3B2)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1–5 µg/mL
ELISA 10 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2a, kappa
Class Monoclonal
Type Antibody
Clone 3B2
Immunogen FGFR1 (NP_000595.1, 303–408 a.a.) partial recombinant protein with GST tag (GST tag MW: 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

Protein sequence:
DNLPYVQILK TAGVNTTDKE MEVLHLRNVS FEDAGEYTCL AGNSIGLSHH SAWLTVLEAL EERPAVMTSP LYLEIIIYCT GAFLISCMVG SVIVYKMKSG TKKSDF

Target Information

FGFR1 (also known as FLT2) belongs to the Fibroblast Growth Factor Receptor family (FGFR1–4), a group of membrane-spanning tyrosine kinases that act as high-affinity receptors for fibroblast growth factors (FGF1–17).
These receptors are involved in key biological processes such as mesoderm induction, cell growth, migration, organ formation, and bone development.
FGFR1 undergoes alternative splicing, resulting in multiple isoforms expressed during embryonic and adult stages.
Mutations or chromosomal aberrations 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 rearrangements involving FGFR1 are linked to stem cell myeloproliferative disorders and stem cell leukemia/lymphoma syndromes.


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

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