Zitierungen und Referenzen (11)

Invitrogen™

BlueJuice™ Gel-Ladepuffer (10x)

BlueJuice Gel-Ladepuffer (10X) ist ein Ladepuffer, der für das einfache Auftragen und Tracking von DNA-Proben auf Agarose- oder nativen PolyacrylamidgelenWeitere Informationen

Katalognummer	Menge
10816015	3 x 1 ml

Katalognummer 10816015

Preis (EUR)

43,65

Exklusiv online

47,66

Ersparnis 4,01 (8%)

Menge:

3 x 1 ml

Großbestellung oder individuelle Größe anfordern

Preis (EUR)

43,65

Exklusiv online

47,66

Ersparnis 4,01 (8%)

BlueJuice Gel-Ladepuffer (10X) ist ein Ladepuffer, der für das einfache Auftragen und Tracking von DNA-Proben auf Agarose- oder nativen Polyacrylamidgelen konzipiert wurde. Die Visualisierung von DNA-Banden wird durch die Tracking-Farbstoffe nicht verdeckt, da sie außerhalb der Grenzen der meisten DNA-Proben liegen.

Produktverwendung
Die empfohlene Konzentration dieses Puffers für die Verwendung mit allen DNA-Proben, die auf Agarose-Gelen laufen, beträgt 1X. Für Acrylamidgele beträgt die empfohlene Konzentration 0,5x.

Nur für Forschungszwecke. Nicht zur Verwendung bei diagnostischen Verfahren.

Specifications

PufferProbenladepuffer

Konzentration10X

GelkompatibilitätAgarose-Gele

Menge3 x 1 ml

Probenladevolumen1 ml

Haltbarkeit6 Monate

VersandbedingungRaumtemperatur

GeltypAgarose

Marker oder FarbstoffBromphenolblau

ProduktlinieBlueJuice

ProdukttypGel-Ladepuffer

Unit SizeEach

Inhalt und Lagerung

• 3 x 1 ml 10X BlueJuice Gel-Ladepuffer

Bis zu 6 Monate bei Raumtemperatur oder 4 °C lagern. Bei längerer Lagerdauer bei –20 °C lagern.

Zitierungen und Referenzen (11)

Zitierungen und Referenzen

Abstract

Cationic glycopolymers for the delivery of pDNA to human dermal fibroblasts and rat mesenchymal stem cells.

Authors:Kizjakina K, Bryson JM, Grandinetti G, Reineke TM

Journal:Biomaterials

PubMed ID:22138032

'Progenitor and pluripotent cell types offer promise as regenerative therapies but transfecting these sensitive cells has proven difficult. Herein, a series of linear trehalose-oligoethyleneamine "click" copolymers were synthesized and examined for their ability to deliver plasmid DNA (pDNA) to two progenitor cell types, human dermal fibroblasts (HDFn) and rat mesenchymal ... More

Comparison of conventional PCR, quantitative PCR, bacteriological culture and the Warthin Starry technique to detect Leptospira spp. in kidney and liver samples from naturally infected sheep from Brazil.

Authors:Fornazari F, da Silva RC, Richini-Pereira VB, Beserra HE, Luvizotto MC, Langoni H

Journal:J Microbiol Methods

PubMed ID:22713608

'Leptospirosis is an infectious disease of worldwide importance. The development of diagnostic techniques allows sick animals to be identified, reservoirs to be eliminated and the disease prevented and controlled. The present study aimed to compare different techniques for diagnosing leptospirosis in sheep. Samples of kidney, liver and blood were collected ... More

Periodontopathogens around the surface of mini-implants removed from orthodontic patients.

Authors:Tortamano A, Dominguez GC, Haddad AC, Nunes FD, Nacao M, Morea C

Journal:Angle Orthod

PubMed ID:22839769

To verify if mini-implant mobility is affected by the presence of periodontopathogens, frequently associated with peri-implantitis.

Microarray-CGH for the assessment of aneuploidy in human polar bodies and oocytes.

Authors:Jaroudi S, Wells D

Journal:Methods Mol Biol

PubMed ID:23138959

The cytogenetic analysis of single cells, such as oocytes and polar bodies, is extremely challenging. The main problem is low probability of obtaining a metaphase preparation in which all of the chromosomes are sufficiently well spread to permit accurate analysis (no overlapping chromosomes, no chromosomes lost). As a result, a ... More

Cloning of cytokine 3' untranslated regions and posttranscriptional assessment using cell-based GFP assay.

Authors:Al-Haj L, Khabar KS

Journal:Methods Mol Biol

PubMed ID:22131027

Cytokine biosynthesis is tightly regulated by a number of processes, including gene expression control. Posttranscriptional control of cytokine gene expression offers a fine-tuning mechanism that contributes not only to transient biosynthesis of cytokines, but also helps in rapid and early initiation of the cytokine response. Deregulation of cytokine biosynthesis has ... More

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