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Merck
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重要文件

F3922

Sigma-Aldrich

Anti-Fibroblast Growth Factor Receptor-3, Extracellular antibody produced in rabbit

affinity isolated antibody, buffered aqueous solution

同義詞:

Anti-FGFR-3

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About This Item

MDL號碼:
分類程式碼代碼:
51111800
NACRES:
NA.41

生物源

rabbit

品質等級

共軛

unconjugated

抗體表格

affinity isolated antibody

抗體產品種類

primary antibodies

無性繁殖

polyclonal

形狀

buffered aqueous solution

分子量

antigen ~120 kDa

物種活性

human

技術

immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:1,000 using protease-digested, human and animal tissue sections
western blot: 1:500 using extract of FGFR-3 transfected cells

UniProt登錄號

運輸包裝

dry ice

儲存溫度

−20°C

目標翻譯後修改

unmodified

基因資訊

human ... FGFR3(2261)

一般說明

FGFR3 (fibroblast growth factor receptor 3) is widely expressed in many fetal and adult human and animal tissues. It belongs to the fibroblast growth factor receptor (Fgfr) family of proteins. It has 19 exons, an extracellular ligand binding domain, a transmembrane domain and an intracellular tyrosine kinase domain. It is located on human chromosome 4p16.3.

免疫原

synthetic peptide corresponding to amino acids 359-372 of the extracellular region of human fibroblast growth factor receptor-3.

應用

Anti-Fibroblast Growth Factor Receptor-3, Extracellular antibody produced in rabbit has been used in:
  • immunoblotting
  • immunohistochemistry
  • immunoprecipitation

生化/生理作用

Fibroblast growth factors (FGFs) are substantially involved in normal development, wound healing and repair, angiogenesis, a variety of neurotrophic activities, and in hematopoiesis as well as in tissue remodeling and maintenance. They have also been implicated in pathological conditions such as tumorigenesis and metastasis. Deletions of chromosome 4p encompassing the FGFR3 (fibroblast growth factor receptor 3) gene cause the Wolf-Hirschhorn syndrome (growth failure, mental retardation, cardiac and bone malformations). Achondroplasia is an inherited disorder in which growth abnormality of bone or cartilage lead to skeletal maldevelopment and dwarfism. It is associated with recurrent mutations of a single amino acid in the transmembrane domain of the FGFR-3 protein.

外觀

Solution in 0.01 M phosphate buffered saline, pH 7.4, containing 1% bovine serum albumin and 15 mM sodium azide.

準備報告

Affinity isolated on a peptide-agarose column.

免責聲明

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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儲存類別代碼

10 - Combustible liquids

水污染物質分類(WGK)

nwg

閃點(°F)

Not applicable

閃點(°C)

Not applicable


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存取文件庫

F R Lamont et al.
British journal of cancer, 104(1), 75-82 (2010-12-02)
Activating mutations of FGFR3 are frequently identified in superficial urothelial carcinoma (UC) and increased expression of FGFR1 and FGFR3 are common in both superficial and invasive UC. The effects of inhibition of receptor activity by three small molecule inhibitors (PD173074
Small molecule FGF receptor inhibitors block FGFR-dependent urothelial carcinoma growth in vitro and in vivo
Lamont FR, et al.
British Journal of Cancer, 104(1), 75-82 (2010)
Fibroblast growth factors: biology, function, and application for tissue regeneration
Yun YR, et al.
Journal of Tissue Engineering, 1(1), 218142-218142 (2010)
Exploring the developmental mechanisms underlying Wolf-Hirschhorn Syndrome: Evidence for defects in neural crest cell migration
Rutherford EL and Lowery LA
Developmental Biology, 420(1), 1-10 (2016)
Loss of heterozygosity at 4p16. 3 and mutation of FGFR3 in transitional cell carcinoma
Sibley K, et al.
Oncogene, 20(6), 686-686 (2001)

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