Human secretogranin-1 (chromogranin-B)(CHGB/SCG1)ELISA kit
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中文名称:人分泌粒蛋白1(嗜铬粒蛋白B)(CHGB/SCG1)酶联免疫试剂盒
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货号:CSB-E17547h
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规格:96T/48T
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价格:¥3600/¥2500
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其他:
产品详情
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别名:CCB peptide ELISA Kit; Cg B ELISA Kit; CgB ELISA Kit; Chgb ELISA Kit; Chromogranin-B ELISA Kit; ChromograninB ELISA Kit; SCG1 ELISA Kit; SCG1_HUMAN ELISA Kit; Secretogranin 1 ELISA Kit; Secretogranin B ELISA Kit; Secretogranin I ELISA Kit; SgI ELISA Kit
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缩写:CHGB
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Uniprot No.:
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种属:Homo sapiens (Human)
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样本类型:serum, plasma, tissue homogenates.
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检测范围:1.56 ng/ml - 100 ng/ml
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灵敏度:0.39 ng/ml
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反应时间:1-5h
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样本体积:50-100ul
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检测波长:450 nm
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研究领域:Neuroscience
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测定原理:quantitative
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测定方法:Sandwich
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数据处理:
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货期:3-5 working days
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靶点详情
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功能:Secretogranin-1 is a neuroendocrine secretory granule protein, which may be the precursor for other biologically active peptides.
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基因功能参考文献:
- evidence suggests that the P413L variant of chromogranin B is not associated with amyotrophic lateral sclerosis (ALS) risk or age at ALS onset (meta-analysis). PMID: 28795874
- Data suggest that chromogranin B (CGB) is a promising emerging biomarker in heart failure (HF) patients with unique potential to integrate information from myocardial stress and neuro-endocrine activation. PMID: 29098879
- Circulating chromogranin B (CgB) levels measured on Intensive Care Unit (ICU) admission provided additional prognostic information to established risk indices in acute respiratory failure (ARF) patients. PMID: 28049363
- results presented here suggest that CHGB variant alleles, the rare CHGB-L413 and common CHGB-P413, may act as modifiers of ALS disease dependent on their expression levels which is higher in females because of a sex-determining region Y element in the CHGB gene promoter. PMID: 28175304
- our results suggest that genetic variants of CHGB may have sex-specific effects on the risk of schizophrenia and provide useful preliminary information for further study. PMID: 28332369
- intracellular calcium binding protein Sg1 is increased in early multiple sclerosis (MS) patients compared to relapsing-remitting MS and neurological controls. PMID: 26152395
- The polymorphism P413L in the CHGB gene was not associated with sporadic amyotrophic lateral sclerosis in a group of Italian patients. PMID: 26003296
- A heterogeneous response to short- and long-term physical activities among circulating granin proteins, particularly chromogranin B. PMID: 23816467
- Results do not support the 413L variant of chromogranin B as a risk factor for sporadic amyotrophic lateral sclerosis in the French population. PMID: 20932227
- common polymorphism in the 3'-UTR (C+84A) of CHGB, which disrupts an A/U-rich messenger ribonucleic acid stability element, associates with not only CHGB secretion but also excretion of isoprostane PMID: 20888525
- The common CHGB promoter variants A-296C and A-261T, and their consequent haplotypes, alter binding of specific transcription factors to influence gene expression in cella as well as BP in vivo PMID: 20359597
- Genetic variation at the CHGB locus, in the proximal promoter, influences CHGB expression as well as catecholamine secretion and later the early heritable responses to environmental stress, and resting/basal Blood Pressure in the population. PMID: 20011129
- finding that CHGB may act as a susceptibility gene and modifier of onset in ALS is consistent with the emerging view that dysfunction of the secretory pathway may contribute to increased vulnerability of motor neurons PMID: 20007371
- Chromogranin B was selected as a candidate gene for schizophrenia. We systematically screened all the promoter and exon regions of the gene and detected 15 single nucleotide polymorphisms in a Chinese population. PMID: 11959426
- CgB may play some role in the early phase of neoplastic progression PMID: 12165659
- there are four different types of chromogranin B in pancreatic islets as demonstrated by region-specific antibodies PMID: 12438147
- 5 CgB fragments were measured in plasma: CgB1-16, CgB312-331, CgB439-451, CgB568-577, & CgB647-657. Substantial heritability, as measured by h2r, was observed for 3 of the fragment concentrations, CgB312-331, CgB439-451, and CgB568-577. PMID: 15138309
- 10 microsatellite markers were analyzed, and an association of schizophrenia was found with D20S882 and D20S905 that flank D20S95. The chromogranin B gene is 30 kb from D20S905. PMID: 15219467
- Overall, our results suggest that at least one locus in or close to the CHGB gene confers risk of the disorder and strengthen the evidence that CHGB is a promising susceptibility gene for schizophrenia in Chinese population. PMID: 17143778
- Locally infused tyramine produced dose-dependent pressor responses, predicted by family history of hypertension, sex, and genetic variants at loci, particularly CHGB, that encode the biosynthesis, storage, and metabolism of catecholamines. PMID: 18180394
- semiquantitative immunocytochemistry for chromogranin B in amyotrophic lateral sclerosis PMID: 18721831
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亚细胞定位:Secreted. Note=Neuroendocrine and endocrine secretory granules.
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蛋白家族:Chromogranin/secretogranin protein family
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组织特异性:Expressed in the adrenal medulla, and in pheochromocytoma. Not expressed in liver.
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数据库链接:
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