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Merck

12039672910

Roche

DIG Northern Starter Kit

greener alternative

suitable for Northern blotting, sufficient for 10 labeling reactions

Synonim(y):

DIG system, Northern blot

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About This Item

Kod UNSPSC:
41105500

zastosowanie

sufficient for 10 blots (blots of 10 x 10 cm2)
sufficient for 10 labeling reactions

Poziom jakości

producent / nazwa handlowa

Roche

charakterystyka ekologicznej alternatywy

Designing Safer Chemicals
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

Parametry

68 °C optimum reaction temp.

metody

Northern blotting: suitable

kategoria ekologicznej alternatywy

temp. przechowywania

−20°C

Opis ogólny

The DIG Northern Starter Kit is designed for the novice DIG system user. It contains the reagents proven to provide successful, reproducible results in northern blots. Additionally, the more convenient forms of standard DIG system products are included (e.g., CDP Star, ready-to-use). The small number of reactions allows the user to gain a firm foundation using the DIG system, then "graduate" to the standard pack sizes. For optimum success, use this kit with the DIG Wash and Block Buffer Set.This kit is used for the generation of single-stranded, DIG-labeled RNA probes and chemiluminescent detection. Labeled probes are synthesized by the in vitro transcription method.
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product is designed as a safer chemical.  The DIG System was established as a sensitive and cost-effective alternative to radioactivity for the labeling and detection of nucleic acids. There are many available publications that prove the versatility of the DIG System, so use of radio-labeling is no longer the only option for labeling of DNA for hybridization.

Zastosowanie

DIG northern starter kit has been used in northern blot hybridization to analyse hepatitis B virus (HBV) RNAs, citrus leprosis virus cytoplasmic type 2 (CiLV-C2) RNAs.
The DIG Northern Starter Kit produces DIG-labeled RNA probes that can be used in conjunction with the supplied chemiluminescent detection reagents for northern blotting techniques. Using linearized DNA as a template, SP6, T3, or T7 RNA Polymerases are used to incorporate DIG-11-UTP into the RNA transcript. After labeling, the DIG-labeled probe is immediately ready for use in hybridization. For convenience, DIG Easy Hyb can be used for hybridization. The DIG Easy Hyb granules are easily reconstituted by adding 64 ml DEPC-treated (RNase-free) water directly to the bottle (once reconstituted, DIG Easy Hyb is stable for 1 month at room temperature). After hybridization, the hybridization solution containing the DIG-labeled RNA probe can be stored at -15 to -25 °C for future re-use (up to 1 year).

Opakowanie

1 kit containing 11 components.
1 kit for up to 10 labeling reactions and detection of 10 blots, blots of 10×10cm2, reactions of μg DNA, yielding approx. 20μg labeled RNA, each
Sensitivity and specificity: Using 1μg of linearized template DNA, the labeling reaction typically yields 20μg of newly synthesized DIG-labeled RNA within 1 hour. The DIG-labeled RNA probe can detect 0.1pg of homologous DNA or RNA in a dot blot. Rare mRNAs can be detected in 0.1μg of total RNA.

Uwaga dotycząca przygotowania

Working solution: Note: Use sterile, RNase-free solutions and equipment
Assay Time: 9 hours 30 minutes
Sample Materials:
  • Linearized plasmid, including the appropriate RNA polymerase promoter sequence (SP6, T3, T7).
  • Specially prepared PCR productWorking solution: Note: Use sterile, RNase-free solutions and equipment.

Note: The length of the region to be transcribed should be in the range of 200 to 1,000 bp. To avoid RNase contamination the DNA must be phenolized.

Inne uwagi

For life science research only. Not for use in diagnostic procedures.
This page may contain text that has been machine translated.

Tylko elementy zestawu

Numer produktu
Opis

  • Labeling Mix 5x concentrated

  • Transcription Buffer 5x concentrated

  • SP6 RNA Polymerase 20 U/μl

  • T7 RNA Polymerase 20 U/μl

  • T3 RNA Polymerase 20 U/μl

  • Anti-Digoxigenin-AP antibody, Fab fragments 750 U/ml

  • DNase I, RNase free 10 U/μl

  • CDP-Star ready-to-use

  • Actin RNA Probe, DIG-labeled Antisense Probe, length 588 bases 10 ng/μl

  • DIG Easy Hyb Granules

  • Blocking Solution 10x concentrated

Zobacz wszystko (11)

Piktogramy

CorrosionExclamation mark

Hasło ostrzegawcze

Danger

Zwroty wskazujące rodzaj zagrożenia

Kod klasy składowania

12 - Non Combustible Liquids

Klasa zagrożenia wodnego (WGK)

WGK 3

Temperatura zapłonu (°F)

does not flash

Temperatura zapłonu (°C)

does not flash


Certyfikaty analizy (CoA)

Poszukaj Certyfikaty analizy (CoA), wpisując numer partii/serii produktów. Numery serii i partii można znaleźć na etykiecie produktu po słowach „seria” lub „partia”.

Masz już ten produkt?

Dokumenty związane z niedawno zakupionymi produktami zostały zamieszczone w Bibliotece dokumentów.

Odwiedź Bibliotekę dokumentów

Interleukin-34 inhibits hepatitis B virus replication in vitro and in vivo
Cheng ST, et al.
PLoS ONE, 12 (2017)
Tuong Vi T Dang et al.
BMC research notes, 7, 655-655 (2014-09-19)
In plants, RNA- based gene silencing mediated by small RNAs functions at the transcriptional or post-transcriptional level to negatively regulate target genes, repetitive sequences, viral RNAs and/or transposon elements. Post-transcriptional gene silencing (PTGS) or the RNA interference (RNAi) approach has
Li Li et al.
International journal of oncology, 48(4), 1541-1552 (2016-02-06)
The metastasis-associated phosphatase of regenerating liver-3 (PRL-3) plays multiple roles in progression of various human cancers; however, significance of its role during development has not been addressed. Here we cloned and characterized the expression pattern of zebrafish prl-3 transcript and
A Novel Virus of the Genus Cilevirus Causing Symptoms Similar to Citrus Leprosis
Roy A, et al.
Phytopathology, 103, 488-500 (2013)
Avijit Roy et al.
Phytopathology, 103(5), 488-500 (2012-12-28)
Citrus leprosis in Colombia was previously shown to be caused by cytoplasmic Citrus leprosis virus (CiLV-C). In 2011, enzyme-linked immunosorbent assay and reverse-transcription polymerase chain reaction (RT-PCR)-based diagnostic methods failed to identify CiLV-C from citrus samples with symptoms similar to

Produkty

Digoxigenin (DIG) labeling methods and kits for DNA and RNA DIG probes, random primed DNA labeling, nick translation labeling, 5’ and 3’ oligonucleotide end-labeling.

Metody znakowania digoksygeniną (DIG) i zestawy do sond DNA i RNA DIG, znakowanie DNA z losowym primerem, znakowanie nickiem translacyjnym, znakowanie końcowe oligonukleotydów 5' i 3'.

Protokoły

DIG Northern Starter Kit Protocol & Troubleshooting

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