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FGF10 (基因名), Fibroblast growth factor 10 (蛋白名), fgf10_human.
产品名称:

Human FGF10/ Fibroblast growth factor 10 Recombinant Protein
成纤维细胞生长因子10

货号:

R1882h

商标:
EIAab®
监管等级:
别名:

Keratinocyte growth factor 2, FGF-10

序列号:
O15520
来源:
E.coli
种属:
Human
标签:
His
序列:
38-208aa
预估分子量:
18.81 kDa (monomer)
纯度:
>90% by SDS-PAGE
浓度:
Reconstitution Dependent
形态:
Liquid
内毒素水平:
Please contact protein@eiaab.com The technician for more information.
应用:
存储缓冲液:
50mM NaH2PO4, 500mM NaCl Buffer with 500mM Imidazole, 10%glycerol(PH8.0)
存储:
Store at -20°C. (Avoid repeated freezing and thawing.)
研究领域:
-
Human FGF10 Protein
规格 & 价格: cart
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Human FGF10 Protein
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产品说明书
说明书: 下载说明书
MSDS: MSDS
在线询价


R&D 技术数据
更多信息,请参阅手册,或联系我们的技术支持: tech@eiaab.com.
基因位点
Cytogenetic band: 5p12 by HGNC 5p12 by Entrez Gene 5p12 by Ensembl
FGF10 Gene in genomic location: bands according to Ensembl, locations according to GeneLoc (and/or Entrez Gene and/or Ensembl if different)
基因位点
通用注释


亚单元:
Interacts with FGFR1 and FGFR2. Interacts with FGFBP1.


功能:
Plays an important role in the regulation of embryonic development, cell proliferation and cell differentiation. Required for normal branching morphogenesis. May play a role in wound healing.


亚细胞位置:
Secreted


该产品尚未在任何出版物中被引用。

[1].
"Structure and expression of human fibroblast growth factor-10."

[2].
"Correlation of the SNPs of FGFR1, FGF10, FGF18 with nonsyndromic cleft lip with or without palate in Chinese population."

[3].
"Association study for genes at chromosome 5p13-q11 in attention deficit hyperactivity disorder."

[4].
"FGFR2, FGF8, FGF10 and BMP7 as candidate genes for hypospadias."

[5].
"Mutations in different components of FGF signaling in LADD syndrome."

[6].
"The fibroblast growth factor binding protein is a novel interaction partner of FGF-7, FGF-10 and FGF-22 and regulates FGF activity: implications for epithelial repair."

[7].
"Structural basis by which alternative splicing confers specificity in fibroblast growth factor receptors."

[8].
"Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study."

[9].
"L-type voltage-dependent calcium channel alpha subunit 1C is a novel candidate gene associated with secondary hyperparathyroidism: an application of haplotype-based analysis for multiple linked single nucleotide polymorphisms."

[10].
"Association between genetic variants of reported candidate genes or regions and risk of cleft lip with or without cleft palate in the polish population."
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