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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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FGFR1 단백질을 인식하는 Mouse monoclonal antibody로 Western blot과 ELISA에 적합. 인간 시료에 반응하며, PBS(pH 7.4) 용액 형태로 제공. 보존제 무첨가, -20°C에서 보관 권장. 연구용으로만 사용 가능.

카탈로그번호
H00002260-M09
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오전 11:33
Thermo Fisher Scientific H00002260-M09 FGFR1 Monoclonal Antibody (1B12) 100 ug pk판매 단위 pk ·
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518,100원VAT 포함 569,910원

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

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1–5 µg/mL
ELISA 0.1 ng/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.) 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

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) belongs to the Fibroblast Growth Factor Receptor (FGFR) family, consisting of four membrane-spanning tyrosine kinases (FGFR1–4) that act as high-affinity receptors for 17 fibroblast growth factors (FGF1–17). These receptors are essential in mesoderm induction, cell growth, migration, organogenesis, and bone development.

FGFR1 undergoes alternative splicing, producing multiple isoforms with distinct expression patterns during embryogenesis and in adult tissues. Mutations or defects in FGFR1 are associated with diseases such as Pfeiffer syndrome, idiopathic hypogonadotropic hypogonadism (IHH), Kallmann syndrome type 2 (KAL2), osteoglophonic dysplasia (OGD), non-syndromic trigonocephaly, Jackson-Weiss syndrome, and 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 or resale without express authorization.

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