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Z175013

Adapter for ACE Micro/Mini-Lab® kit

Mini adapter

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About This Item

UNSPSC Code:
41121815
NACRES:
NB.43

joint

joint ST/NS14/10

manufacturer/tradename

Ace Glass 502825

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General description

With threaded nylon bushing to accommodate 6.5 to 7 mm diam. thermometer or tubing.

Legal Information

Micro/Mini-Lab is a registered trademark of Ace Glass, Inc.

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Giovanna Trinchese et al.
The Journal of nutritional biochemistry, 26(11), 1136-1146 (2015-06-30)
Different nutritional components are able, by modulating mitochondrial function and gut microbiota composition, to influence body composition, metabolic homeostasis and inflammatory state. In this study, we aimed to evaluate the effects produced by the supplementation of different milks on energy
Y Y Xiao et al.
Epidemiology and infection, 143(9), 1833-1838 (2014-11-02)
No published studies have discussed details of the prognosis and survival of patients with severe avian influenza A(H7N9) infection. In this study we analysed 128 laboratory-confirmed cases of severe H7N9 infection in Zhejiang province, the most affected region during the
Mark Zeller et al.
Molecular biology and evolution, 32(8), 2060-2071 (2015-04-11)
The majority of human group A rotaviruses possess the P[8] VP4 genotype. Recently, a genetically distinct subtype of the P[8] genotype, also known as OP354-like P[8] or lineage P[8]-4, emerged in several countries. However, it is unclear for how long
James Neil Fisher et al.
Oncotarget, 6(15), 13176-13200 (2015-05-12)
SKBR3-cells, characterized by ERBB2/RARA co-amplification, represent a subgroup of HER2+ breast-cancers sensitive to all-trans retinoic acid (ATRA) and Lapatinib. In this model, the two agents alone or in combination modulate the expression of 174 microRNAs (miRs). These miRs and predicted
Monique Silvy et al.
Transfusion, 55(6 Pt 2), 1407-1410 (2014-11-22)
The rare amorph Rhnull phenotype is caused by silent alleles at the RH locus and usually arises in consanguineous families. To date, only five molecular backgrounds have been identified in five unrelated families. Subjects with Rhnull red blood cells (RBCs)

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