추천 제품
제조업체/상표
Novagen®
저장 조건
OK to freeze
저장 온도
10-30°C
일반 설명
The BCA protein assay is a simple and reliable protein quantification method.
The BCA protein assay is based on a biuretreaction, which is the reduction of Cu2+ toCu+ by proteins in an alkaline solution withconcentration-dependent detection of themonovalent copper ions. Bicinchoninic acidis a chromogenic reagent that chelates thereduced copper, producing a purple complexwith strong absorbance at 562 nm (Smith1985, Wiechelman 1988). This assay can beused to quantify protein concentration with awide variety of samples and can be performedin minutes.
The Novagen® BCA Protein Assay Kit canbe used to determine protein concentrationin the range of 20-2000 µg/ml in either astandard assay or microassay configuration.Kit components are sufficient to complete500 standard-size reactions (50 µl proteinsample plus 1 ml reagent) or 2500 micro-scalereactions (25 µl protein sample plus 200 µlreagent). A BSA standard (2 mg/ml) is providedfor convenient and reliable preparation ofstandard curves.
This assay is robust and can be performedin the presence of many compounds. Somereagents, including chelating agents, strongacids or bases, and reducing agents, interferewith the reduction and chelating reactions onwhich this assay depends (Brown 1989). TheBCA assay is compatible with the followingNovagen protein extraction and lysis reagents:BugBuster Protein Extraction Reagent,PopCulture Reagent, CytoBuster ProteinExtraction Reagent, Reportasol ExtractionBuffer, and Insect PopCulture Reagent. Optionsfor the removal or dilution of interferingsubstances are described in the kit literature.
The Novagen® BCA Protein Assay Kit canbe used to determine protein concentrationin the range of 20-2000 µg/ml in either astandard assay or microassay configuration.Kit components are sufficient to complete500 standard-size reactions (50 µl proteinsample plus 1 ml reagent) or 2500 micro-scalereactions (25 µl protein sample plus 200 µlreagent). A BSA standard (2 mg/ml) is providedfor convenient and reliable preparation ofstandard curves.
This assay is robust and can be performedin the presence of many compounds. Somereagents, including chelating agents, strongacids or bases, and reducing agents, interferewith the reduction and chelating reactions onwhich this assay depends (Brown 1989). TheBCA assay is compatible with the followingNovagen protein extraction and lysis reagents:BugBuster Protein Extraction Reagent,PopCulture Reagent, CytoBuster ProteinExtraction Reagent, Reportasol ExtractionBuffer, and Insect PopCulture Reagent. Optionsfor the removal or dilution of interferingsubstances are described in the kit literature.
성분
•500 mlBCA Solution
•15 ml4% Cupric Sulfate
•3 x 1 mlBSA Standard, 2 mg/ml
•15 ml4% Cupric Sulfate
•3 x 1 mlBSA Standard, 2 mg/ml
경고
Toxicity: Multiple Toxicity Values, refer to MSDS (O)
기타 정보
Smith, P.K., et al. 1985. Anal. Biochem.150, 76.
Kessler, R. J. and Fanestil, D. D. 1986. Anal. Biochem 159, 138.
Wiechelman, K., et al. 1988. Anal. Biochem.175, 231.
Brown, R., et al. 1989. Anal. Biochem.180, 136.
Kessler, R. J. and Fanestil, D. D. 1986. Anal. Biochem 159, 138.
Wiechelman, K., et al. 1988. Anal. Biochem.175, 231.
Brown, R., et al. 1989. Anal. Biochem.180, 136.
법적 정보
Use of the BCA protein assay is permitted for research purposes only.
NOVAGEN is a registered trademark of Merck KGaA, Darmstadt, Germany
신호어
Danger
유해 및 위험 성명서
Hazard Classifications
Aquatic Acute 1 - Aquatic Chronic 1 - Eye Dam. 1
Storage Class Code
10 - Combustible liquids
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
Shuhan Liu et al.
Oxidative medicine and cellular longevity, 2021, 7674565-7674565 (2021-12-18)
Cysteine metabolism plays a critical role in cancer cell survival. Cysteine depletion was reported to inhibit tumor growth and induce pancreatic cancer cell ferroptosis. Nevertheless, the effect of cysteine depletion in chronic myeloid leukemia (CML) remains to be explored. In
Roberta Gonnella et al.
Microbes and infection, 22(10), 585-591 (2020-09-04)
Viral egress and autophagy are two mechanisms that seem to be strictly connected in Herpesviruses's biology. Several data suggest that the autophagic machinery facilitates the egress of viral capsids and thus the production of new infectious particles. In the Herpesvirus
Abdullah S Shatoor et al.
Saudi journal of biological sciences, 28(12), 7012-7021 (2021-12-07)
This study evaluated the protective effect of astaxanthin (ASX) against high-fat diet (HFD)-induced cardiac damage and fibrosis in rats and examined if the mechanism of protection involves modulating SIRT1. Rat were divided into 5 groups (n = 10/group) as: 1) control: fed
Ranjithmenon Muraleedharan et al.
Cell reports, 32(9), 108092-108092 (2020-09-03)
Lactate is used as an energy source by producer cells or shuttled to neighboring cells and tissues. Both glucose and lactate fulfill the bioenergetic demand of neurons, the latter imported from astrocytes. The contribution of astrocytic lactate to neuronal bioenergetics
자사의 과학자팀은 생명 과학, 재료 과학, 화학 합성, 크로마토그래피, 분석 및 기타 많은 영역을 포함한 모든 과학 분야에 경험이 있습니다..
고객지원팀으로 연락바랍니다.