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Thermo Fisher Scientific Phospho-FGFR1 (Tyr776) Polyclonal Antibody, Biotin
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Thermo Fisher Scientific Phospho-FGFR1 (Tyr776) Polyclonal Antibody, Biotin

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FGFR1 단백질의 Tyr776 인산화 부위를 특이적으로 인식하는 Biotin 결합 다클론 항체. Western blot, ELISA, IP에 사용 가능하며 사람 및 랫드 시료에 반응. 고순도 친화 크로마토그래피 정제, 안정한 보관을 위한 글리세롤 및 BSA 포함.

카탈로그번호
PFGFR1-BIOTIN
판매단위
pk
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마지막 업데이트 2025. 08. 04. 오후 01:50
Thermo Fisher Scientific PFGFR1-BIOTIN Phospho-FGFR1 (Tyr776) Polyclonal Antibody, Biotin 200 ul pk판매 단위 pk ·
재고 확인 필요
669,600원VAT 포함 736,560원

Thermo Fisher Scientific · Thermo Fisher Scientific Phospho-FGFR1 (Tyr776) Polyclonal Antibody, Biotin

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:500–1:1,000
ELISA 1:10,000
Immunoprecipitation (IP) 1:50–1:250

Product Specifications

항목 내용
Species Reactivity Human, Rat
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen Synthetic peptide taken within amino acid region 640–690 on human basic fibroblast growth factor receptor protein 1
Conjugate Biotin
Form Liquid
Concentration 0.5–1.5 mg/mL
Purification Affinity chromatography
Storage Buffer Proprietary buffer, pH 7.4–7.8, with 30% glycerol, 0.5% BSA
Contains 0.02% sodium azide
Storage Conditions −20°C
Shipping Conditions Ambient (domestic); Wet ice (international)

Target Information

FGFR1 (also known as FLT2) is a member of the Fibroblast Growth Factor Receptor (FGFR) family, a group of four membrane-spanning tyrosine kinases (FGFR1–4) that serve as high-affinity receptors for 17 growth factors (FGF1–17).
The FGF receptor family plays an important role in multiple biological processes, including mesoderm induction and patterning, cell growth and migration, organ formation, and bone growth.
FGFR1 undergoes alternative splicing, generating multiple variants that are differentially expressed 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, and Antley-Bixler syndrome.
Chromosomal aberrations involving FGFR1 are also 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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