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Citations & References (11)
Invitrogen™
BlueJuice™ Gel Loading Buffer (10X)
BlueJuice Gel Loading Buffer (10X) is designed for easy loading and tracking of DNA samples in agarose or native polyacrylamideRead more
| Catalog Number | Quantity |
|---|---|
| 10816015 | 3 x 1 mL |
Catalog number 10816015
Price (EUR)
42,65
Online Exclusive
46,53Save 3,88 (8%)
Each
Quantity:
3 x 1 mL
Price (EUR)
42,65
Online Exclusive
46,53Save 3,88 (8%)
Each
BlueJuice Gel Loading Buffer (10X) is designed for easy loading and tracking of DNA samples in agarose or native polyacrylamide gels. Visualization of DNA bands will not be obscured by the tracking dyes because they run outside the limits of most DNA samples.
Product use
The recommended concentration of this buffer for use with all DNA samples run on agarose gels is 1X. For acrylamide gels, the recommended concentration is 0.5 X.
Product use
The recommended concentration of this buffer for use with all DNA samples run on agarose gels is 1X. For acrylamide gels, the recommended concentration is 0.5 X.
For Research Use Only. Not for use in diagnostic procedures.
Specifications
BufferSample Loading Buffers
Concentration10X
Gel CompatibilityAgarose Gels
Product LineBlueJuice
Product TypeGel Loading Buffer
Quantity3 x 1 mL
Sample Loading Volume1 mL
Shelf Life6 Months
Shipping ConditionRoom Temperature
Gel TypeAgarose
Label or DyeBromophenol Blue
Unit SizeEach
Contents & Storage
• 3 x 1 mL 10X BlueJuice Gel Loading Buffer
Store at room temperature or at 4°C for up to 6 months. For longer periods, store at -20°C.
Store at room temperature or at 4°C for up to 6 months. For longer periods, store at -20°C.
Citations & References (11)
Citations & References
Abstract
Cationic glycopolymers for the delivery of pDNA to human dermal fibroblasts and rat mesenchymal stem cells.
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
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.
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
Periodontopathogens around the surface of mini-implants removed from orthodontic patients.
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.
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
Cloning of cytokine 3' untranslated regions and posttranscriptional assessment using cell-based GFP assay.
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