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CST3 抗体

This anti-CST3 antibody is a 小鼠 单克隆 antibody detecting CST3 in ELISA 和 IHC. Suitable for 人. This Primary Antibody has been cited in 17+ publications.
产品编号 ABIN1045447
发货至: 中国

Quick Overview for CST3 抗体 (ABIN1045447)

抗原

See all CST3 抗体
CST3 (Cystatin C (CST3))

适用

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宿主

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小鼠

克隆类型

  • 95
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单克隆

标记

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This CST3 antibody is un-conjugated

应用范围

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ELISA, Immunohistochemistry (IHC)

克隆位点

3A1B7
  • 特异性

    Specific for Human Cystatin C denatured and native forms

    交叉反应

    纯化方法

    Protein G purified

    免疫原

    Recombinant Human Cystatin C protein

    亚型

    IgG2b
  • 应用备注

    Recommended dilution:IHC:1:50-1:500,

    说明

    Other species are not tested. Please decide the specificity by homology

    限制

    仅限研究用
  • 状态

    Liquid

    缓冲液

    Preservative: 0.03 % Proclin 300
    Constituents: 50 % Glycerol, 0.01M PBS, PH 7.4

    储存液

    ProClin

    注意事项

    This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

    注意事项

    Avoid freeze and thaw cycles.

    储存条件

    -20 °C,-80 °C

    储存方法

    Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
  • Targońska-Stepniak, Majdan: "Cystatin C concentration is correlated with disease activity in rheumatoid arthritis patients." in: Scandinavian journal of rheumatology, Vol. 40, Issue 5, pp. 341-6, (2011) (PubMed).

    López Gómez, Sacristán Enciso, Micó, Arias Meneses, de Sande Medel, Alejo: "Serum cystatin C and microalbuminuria in the detection of vascular and renal damage in early stages." in: Nefrología : publicación oficial de la Sociedad Española Nefrologia, Vol. 31, Issue 5, pp. 560-6, (2011) (PubMed).

    Warwas, Piwowar: "[Urinary cystatin C as a biomarker of renal tubular injury]." in: Postȩpy higieny i medycyny doświadczalnej (Online), Vol. 65, pp. 562-8, (2011) (PubMed).

    Reznichenko, Panphilova, Evdokimova, Osmolovskaia, Chumakova, Dankovtseva, Baklanova, Barinov, Sidorenko, Zateĭshchikov: "[Cystatin C level is independently related to risk of unfavorable outcome after acute coronary syndrome in individuals with normal or moderately reduced renal function]." in: Kardiologiia, Vol. 51, Issue 6, pp. 4-10, (2011) (PubMed).

    Ito, Pacold, Durazo-Arvizu, Liu, Shilipak, Goff, Tracy, Kramer: "The effect of including cystatin C or creatinine in a cardiovascular risk model for asymptomatic individuals: the multi-ethnic study of atherosclerosis." in: American journal of epidemiology, Vol. 174, Issue 8, pp. 949-57, (2011) (PubMed).

    Borges, Hirota, Quinto, Ribeiro, Zanella, Batista: "Is cystatin C a useful marker in the detection of diabetic kidney disease?" in: Nephron. Clinical practice, Vol. 114, Issue 2, pp. c127-34, (2010) (PubMed).

    Spanaus, Kollerits, Ritz, Hersberger, Kronenberg, von Eckardstein,: "Serum creatinine, cystatin C, and beta-trace protein in diagnostic staging and predicting progression of primary nondiabetic chronic kidney disease." in: Clinical chemistry, Vol. 56, Issue 5, pp. 740-9, (2010) (PubMed).

    Shlipak, Katz, Kestenbaum, Fried, Newman, Siscovick, Stevens, Sarnak: "Rate of kidney function decline in older adults: a comparison using creatinine and cystatin C." in: American journal of nephrology, Vol. 30, Issue 3, pp. 171-8, (2009) (PubMed).

    Muntner, Vupputuri, Coresh, Uribarri, Fox: "Metabolic abnormalities are present in adults with elevated serum cystatin C." in: Kidney international, Vol. 76, Issue 1, pp. 81-8, (2009) (PubMed).

    Hojs, Bevc, Ekart, Gorenjak, Puklavec: "Serum cystatin C-based equation compared to serum creatinine-based equations for estimation of glomerular filtration rate in patients with chronic kidney disease." in: Clinical nephrology, Vol. 70, Issue 1, pp. 10-7, (2008) (PubMed).

    Delanaye, Cavalier, Radermecker, Paquot, Depas, Chapelle, Scheen, Krzesinski: "Cystatin C or creatinine for detection of stage 3 chronic kidney disease in anorexia nervosa." in: Nephron. Clinical practice, Vol. 110, Issue 3, pp. c158-63, (2008) (PubMed).

    Yang, Peng, Lin, Wang, Huang: "Use of serum cystatin C to detect early decline of glomerular filtration rate in type 2 diabetes." in: Internal medicine (Tokyo, Japan), Vol. 46, Issue 12, pp. 801-6, (2007) (PubMed).

    Pucci, Triscornia, Lucchesi, Fotino, Pellegrini, Pardini, Miccoli, Del Prato, Penno: "Cystatin C and estimates of renal function: searching for a better measure of kidney function in diabetic patients." in: Clinical chemistry, Vol. 53, Issue 3, pp. 480-8, (2007) (PubMed).

    Hojs, Bevc, Ekart, Gorenjak, Puklavec: "Serum cystatin C as an endogenous marker of renal function in patients with mild to moderate impairment of kidney function." in: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association, Vol. 21, Issue 7, pp. 1855-62, (2006) (PubMed).

    Shlipak, Katz, Sarnak, Fried, Newman, Stehman-Breen, Seliger, Kestenbaum, Psaty, Tracy, Siscovick: "Cystatin C and prognosis for cardiovascular and kidney outcomes in elderly persons without chronic kidney disease." in: Annals of internal medicine, Vol. 145, Issue 4, pp. 237-46, (2006) (PubMed).

    Mussap, Dalla Vestra, Fioretto, Saller, Varagnolo, Nosadini, Plebani: "Cystatin C is a more sensitive marker than creatinine for the estimation of GFR in type 2 diabetic patients." in: Kidney international, Vol. 61, Issue 4, pp. 1453-61, (2002) (PubMed).

    Basile, Drüeke, Lacour, Ulmann, Bourdeau, Utzinger, Dubost: "Total parathyroidectomy and delayed parathyroid autotransplantation using a simplified cryopreservation technique: human and animal studies." in: American journal of kidney diseases : the official journal of the National Kidney Foundation, Vol. 3, Issue 5, pp. 366-70, (1984) (PubMed).

  • 抗原

    CST3 (Cystatin C (CST3))

    别名

    CST3

    背景

    Background: Defects in CST3 are the cause of amyloidosis type 6 (AMYL6) [MIM:105150], also known as hereditary cerebral hemorrhage with amyloidosis (HCHWA), cerebral amyloid angiopathy (CAA) or cerebroarterial amyloidosis Icelandic type. AMYL6 is a hereditary generalized amyloidosis due to cystatin C amyloid deposition. Cystatin C amyloid accumulates in the walls of arteries, arterioles, and sometimes capillaries and veins of the brain, and in various organs including lymphoid tissue, spleen, salivary glands, and seminal vesicles. Amyloid deposition in the cerebral vessels results in cerebral amyloid angiopathy, cerebral hemorrhage and premature stroke. Cystatin C levels in the cerebrospinal fluid are abnormally low.Genetic variations in CST3 are associated with age-related macular degeneration type 11 (ARMD11) [MIM:611953]. ARMD is a multifactorial eye disease and the most common cause of irreversible vision loss in the developed world. In most patients, the disease is manifest as ophthalmoscopically visible yellowish accumulations of protein and lipid that lie beneath the retinal pigment epithelium and within an elastin-containing structure known as Bruch membrane.

    Aliases: CysC,Cystatin-3,Gamma-trace,Neuroendocrine basic polypeptide,Post-gamma-globulin

    UniProt

    P01034
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