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Thermo Fisher Scientific FGFR2 Recombinant Rabbit Monoclonal Antibody (JM10-60)
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Thermo Fisher Scientific FGFR2 Recombinant Rabbit Monoclonal Antibody (JM10-60)

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FGFR2 단백질을 인식하는 재조합 토끼 단클론 항체로, Western blot과 면역침강(IP)에 적합. 높은 특이성과 재현성을 제공하며, 로트 간 일관성이 우수함. 단백질 A로 정제된 액상 제품으로 4°C 또는 -20°C에서 안정적으로 보관 가능.

카탈로그번호
MA532629
판매단위
pk
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마지막 업데이트 2025. 08. 05. 오후 04:56
Thermo Fisher Scientific MA532629 FGFR2 Recombinant Rabbit Monoclonal Antibody (JM10-60) 100 ul pk판매 단위 pk ·
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618,800원VAT 포함 680,680원

Thermo Fisher Scientific · Thermo Fisher Scientific FGFR2 Recombinant Rabbit Monoclonal Antibody (JM10-60)

Applications and Tested Dilution

Application Tested Dilution
Western Blot (WB) 1:1,000–1:2,000
Immunoprecipitation (IP) 1:10–1:50

Product Specifications

항목 내용
Species Reactivity Human, Mouse, Rat
Host / Isotype Rabbit / IgG
Expression System HEK293 cells
Class Recombinant Monoclonal
Type Antibody
Clone JM10-60
Immunogen Synthetic peptide within Human FGFR2 (aa 30–70)
Conjugate Unconjugated
Form Liquid
Concentration 1 mg/mL
Purification Protein A
Storage Buffer TBS, pH 7.4, with 40% Glycerol, 0.05% BSA
Contains 0.05% sodium azide
Storage Conditions Store at 4°C short term. For long term storage, store at -20°C, avoiding freeze/thaw cycles.
Shipping Conditions Wet ice
RRID AB_2809906

Product Specific Information

Recombinant rabbit monoclonal antibodies are produced using in vitro expression systems. The antibody DNA sequences from immunoreactive rabbits are cloned and expressed, followed by screening to select optimal clones for production.
Advantages include:

  • High specificity and sensitivity
  • Lot-to-lot consistency
  • Animal origin-free formulation
  • Broader immunoreactivity due to the large rabbit immune repertoire

Target Information

FGFR2 (Fibroblast Growth Factor Receptor 2) is a receptor tyrosine kinase that regulates diverse cellular functions such as angiogenesis, mitogenesis, osteogenesis, myogenesis, carcinogenesis, differentiation, and tissue repair.
It is implicated in diseases including cancer, rheumatoid arthritis, and diabetic retinopathy.
Mutations in FGFR2 are associated with several syndromes, including:

  • Crouzon syndrome
  • Pfeiffer syndrome
  • Craniosynostosis
  • Apert syndrome
  • Jackson-Weiss syndrome
  • Beare-Stevenson cutis gyrata syndrome
  • Saethre-Chotzen syndrome

Multiple alternatively spliced transcript variants encoding different isoforms have been identified.


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

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