Thermo Fisher Scientific FGFR1 Monoclonal Antibody (VBS-7)
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카탈로그 번호 | CAS 번호 | 설명 | 상태 | 단위 | 판매가 | 할인가 | 가격(VAT포함) | 수량 / 장바구니 / 찜 |
133100 | - | Thermo Fisher Scientific 133100 FGFR1 Monoclonal Antibody (VBS-7) 100 ug pk | 재고문의 | pk | 606,000원 | - | 666,600원 |
다른 상품 둘러보기
Applications
Tested Dilution
Publications
Western Blot (WB)
2 µg/mL
View 2 publications 2 publications
Immunohistochemistry (IHC)
-
View 1 publication 1 publication
Immunohistochemistry (Paraffin) (IHC (P))
1:20-1:200
Immunocytochemistry (ICC/IF)
-
View 2 publications 2 publications
Flow Cytometry (Flow)
-
View 1 publication 1 publication
ELISA (ELISA)
0.1-1.0 µg/mL
Immunoprecipitation (IP)
2-5 µg
Product Specifications
Species Reactivity
Bovine, Chicken, Guinea pig, Human, Mouse, Rat
Published species
Human, Mouse, Rabbit
Host/Isotype
Mouse / IgG1
Class
Monoclonal
Type
Antibody
Clone
VBS-7
Immunogen
Bovine FGF Receptor 1 (flg) purified from bovine Coronary Venular Endothelial Cells (CVEC).
Conjugate
Unconjugated Unconjugated Unconjugated
Form
Liquid
Concentration
0.5 mg/mL
Purification
purified
Storage buffer
PBS
Contains
0.1% sodium azide
Storage conditions
-20°C
Shipping conditions
Ambient (domestic); Wet ice (international)
RRID
AB_2533011
Target Information
FGFR1 (also known as FLT2) is a member of the Fibroblast Growth Factor Receptor family that constitute a family of four membrane-spanning tyrosine kinases (FGFR1-4) which 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 is alternatively spliced generating multiple splice variants that are differentially expressed during embryo development and in the adult body. Other defects in FGFR1 are responsible for several diseases which include 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 this gene 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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