추천 제품
사용
sufficient for 10 blots (blots of 10 x 10 cm2)
sufficient for 10 labeling reactions
Quality Level
제조업체/상표
Roche
환경친화적 대안 제품 특성
Designing Safer Chemicals
Learn more about the Principles of Green Chemistry.
sustainability
Greener Alternative Product
파라미터
68 °C optimum reaction temp.
기술
Northern blotting: suitable
환경친화적 대안 카테고리
저장 온도
−20°C
일반 설명
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.
애플리케이션
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).
포장
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
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.
제조 메모
Working solution: Note: Use sterile, RNase-free solutions and equipment
Assay Time: 9 hours 30 minutes
Sample Materials:
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.
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.
기타 정보
For life science research only. Not for use in diagnostic procedures.
키트 구성품 전용
제품 번호
설명
- 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
모두 보기 (11)
신호어
Danger
유해 및 위험 성명서
Storage Class Code
12 - Non Combustible Liquids
WGK
WGK 3
Flash Point (°F)
does not flash
Flash Point (°C)
does not flash
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.
이미 열람한 고객
Interleukin-34 inhibits hepatitis B virus replication in vitro and in vivo
PLoS ONE, 12 (2017)
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
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
Phytopathology, 103, 488-500 (2013)
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
문서
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.
프로토콜
DIG Northern Starter Kit Protocol & Troubleshooting
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