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Merck
CN

SAB4200663

Sigma-Aldrich

Anti-Copeptin antibody produced in rabbit

affinity isolated antibody

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别名:
CT-proAVP
UNSPSC代码:
51111800
NACRES:
NA.41

生物来源

rabbit

质量水平

抗体形式

affinity isolated antibody

抗体产品类型

primary antibodies

种属反应性

human

浓度

~1 mg/mL

技术

immunoblotting: 0.25-0.5  μg/mL (recommended using recombinant human Copeptin trifluoroacetate)
immunohistochemistry: 20 μg/mL (recommended using mouse or human kidney sections)
immunoprecipitation (IP): 5-10 μg (recommended using recombinant human Copeptin trifluoroacetate (C8749).)
indirect ELISA: 0.25-0.5  μg/mL (recommended using human Copeptin trifluoroacetate (C8749) for coating.)

UniProt登记号

运输

dry ice

储存温度

−20°C

靶向翻译后修饰

unmodified

基因信息

human ... AVP(551)

相关类别

一般描述

AVP or pre-proAVP, also known as, vasopressin-neurophysin 2-copeptin is one of the main hormones of the axis hypothalamic-pituitary adrenal. It is split into 3 chains: Arg-vasopressin, neurophysin-2 and copeptin. Copeptin is a glycopeptide with 39 amino acids, located at the C-terminal part of the pre-proAVP. It is secreted by the posterior pituitary gland and poured into the systemic circulation.
The gene AVP (arginine vasopressin) is mapped to human chromosome 20. It is an antidiurectic hormone which is produced by hypothalamic neurons.

免疫原

a synthetic peptide corresponding to the C-terminal region of human Copeptin

应用

Anti-Copeptin antibody produced in rabbit has been used in various immunochemical techniques including :
  • immunohistochemistry
  • immunoblotting
  • immunoprecipitation
  • enzyme linked immunosorbent assay (ELISA)

生化/生理作用

Copeptin concentration directly reflects AVP activation and serves as a biomarker of the AVP system. Altered copeptin levels are implicated in stroke, sudden death and cardiovascular events. It can also be used as a biomarker for a list of illnesses, such as acute myocardial infarction (AMI), vasodilatory shock, metabolic syndrome, diabetes insipidus, diabetes mellitus, sepsis, septic shock, lower respiratory tract infections, hyponatremia, acute dyspnea, autosomal dominant polycystic kidney disease (ADPKD), intracerebral hemorrhage, pulmonary arterial hypertension (PAH) and head injury.
The gene AVP (arginine vasopressin) encodes preprovasopressin which is processed into vasopressin, neurophysin II and glycoprotein (copeptin). Mutations in it are associated with neurohypophyseal diabetes insipidus. It also plays a crucial role in social mannerism, such as recognition, aggression, reproduction and parenting. The levels of circulating copeptin is higher in children suffering from febrile seizures.

外形

Solution in 0.01 M phos­phate buffered saline, pH 7.4, containing 15 mM sodium azide.

免责声明

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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Benjamin Stöcklin et al.
PloS one, 10(4), e0124663-e0124663 (2015-04-22)
Accurate diagnosis of febrile seizures in children presenting after paroxysmal episodes associated with fever, is hampered by the lack of objective postictal biomarkers. The aim of our study was to investigate whether FS are associated with increased levels of serum
Copeptin and its potential role in diagnosis and prognosis of various diseases
Dobvsa L and Cullen EK
Biochemical Medicine, 23(2), 172-190 (2013)
Jia Jia Liu et al.
PloS one, 10(8), e0136436-e0136436 (2015-08-22)
Arginine vasopressin (AVP) plays a role in social behavior, through receptor AVPR1A. The promoter polymorphism AVPR1A RS3 has been associated with human social behaviors, and with acute response to stress. Here, the relationships between AVPR1A RS3, early-life stressors, and social
M Ito et al.
The Journal of clinical investigation, 91(6), 2565-2571 (1993-06-01)
A transition of G to A at nucleotide position 279 in exon 1 of the vasopressin gene has been identified in patients with familial central diabetes insipidus. The mutation predicts an amino acid substitution of Thr (ACG) for Ala (GCG)
S Rittig et al.
American journal of human genetics, 58(1), 107-117 (1996-01-01)
Familial neurohypophyseal diabetes insipidus (FNDI) is an autosomal dominant disorder characterized by progressive postnatal deficiency of arginine vasopressin as a result of mutation in the gene that encodes the hormone. To determine the extent of mutations in the coding region

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