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Thermo Fisher Scientific FGFR1 Monoclonal Antibody (1B12)
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Thermo Fisher Scientific FGFR1 Monoclonal Antibody (1B12)

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인간 FGFR1 단백질을 표적으로 하는 Thermo Fisher Scientific의 Mouse Monoclonal Antibody (Clone 1B12). Western blot 및 ELISA에 적합하며, PBS 기반 액상 형태로 제공. -20°C 보관, 연구용으로만 사용.

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마지막 업데이트 2025. 08. 05. 오후 05:07
Thermo Fisher Scientific H00002260-M09J FGFR1 Monoclonal Antibody (1B12) 100 ug pk판매 단위 pk ·
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786,900원VAT 포함 865,590원

Thermo Fisher Scientific · Thermo Fisher Scientific FGFR1 Monoclonal Antibody (1B12)

Applications

Western Blot (WB)

  • Assay-Dependent

ELISA

  • 10 µg/mL

Product Specifications

항목 내용
Species Reactivity Human
Host / Isotype Mouse / IgG2b, kappa
Class Monoclonal
Type Antibody
Clone 1B12
Immunogen FGFR1 (NP_000595.1, 303–408 a.a) full-length 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

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 is involved in critical biological processes such as mesoderm induction, cell growth, migration, organ formation, and bone development.
FGFR1 undergoes alternative splicing, generating multiple variants expressed during embryonic development and in adults.
Defects in FGFR1 are linked to various 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 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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