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GNRH1 (基因名), Progonadoliberin-1 (蛋白名), gon1_human.
产品名称:

Human GNRH1/ Progonadoliberin-1 Recombinant Protein
促性腺激素释放激素

货号:

R0843h

商标:
EIAab®
监管等级:
别名:

Progonadoliberin I, GNRH, GRH, LHRH

序列号:
P01148
来源:
E.coli
种属:
Human
标签:
His
序列:
1-92aa
预估分子量:
10.12 kDa (monomer)
纯度:
Greater than 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:
Signal Transduction
  • Human GNRH1 Protein
  • Human GNRH1 Protein
  • Human GNRH1 Protein
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Human GNRH1 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
Human GNRH1 Protein
The PCR product of human GNRH1 gene was determined by 1% Agarose stained with EB.
Human GNRH1 Protein
Recombinant human GNRH1 protein was determined by 12% SDS-PAGE stained with Coomassie Blue under reducing conditions.
基因位点
Cytogenetic band: 8p21.2 by HGNC 8p21.2 by Entrez Gene 8p21.2 by Ensembl
GNRH1 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:
N/A


功能:
Stimulates the secretion of gonadotropins; it stimulates the secretion of both luteinizing and follicle-stimulating hormones.


亚细胞位置:
Secreted



[1].
"Genetic polymorphisms of the GNRH1 and GNRHR genes and risk of breast cancer in the National Cancer Institute Breast and Prostate Cancer Cohort Consortium (BPC3)."

[2].
"Characterization of cDNA for precursor of human luteinizing hormone releasing hormone."

[3].
"Comprehensive analysis of common genetic variation in 61 genes related to steroid hormone and insulin-like growth factor-I metabolism and breast cancer risk in the NCI breast and prostate cancer cohort consortium."

[4].
"A large-scale candidate gene association study of age at menarche and age at natural menopause."

[5].
"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."

[6].
"Screening of autosomal gene deletions in patients with hypogonadotropic hypogonadism using multiplex ligation-dependent probe amplification: detection of a hemizygosis for the fibroblast growth factor receptor 1."

[7].
"Identification of new putative susceptibility genes for several psychiatric disorders by association analysis of regulatory and non-synonymous SNPs of 306 genes involved in neurotransmission and neurodevelopment."

[8].
"High-density association study of 383 candidate genes for volumetric BMD at the femoral neck and lumbar spine among older men."

[9].
"GNRH1 mutations in patients with idiopathic hypogonadotropic hypogonadism."

[10].
"Isolated familial hypogonadotropic hypogonadism and a GNRH1 mutation."
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