경신과학

Zymo Research

▪ HOME>제품정보>Zymo Research

RNA Clean & Concentrator-5

• Quick methods for cleaning and concentrating RNA.
• Zymo-Spin™ Column/Plate technology allows minimal elution volumes.
• Ideal for purification of RNA from aqueous phase following acid phenol extraction.

서한형 대리

Zymo Research 제품 담당자

경신과학(주)

영업부

H.P) 010-8832-6303

HanHyung Seo

Zymo Research Brand Manager

Kyongshin scientific Co., Ltd.

Sales Department

H.P) 82)10-8832-6303

제품소개

RNA Clean and Concentrator Protocol:

hIGHLIGHTS

NGS-Ready: RNA is ready for all downstream applications including Next-Gen Sequencing, RT-qPCR, hybridization, etc.
Ultra-Pure: Eliminate contaminants and inhibitors in 5 minutes.
Maximum Recovery: Recover >90% and elute in as little as 6 μl.

DESCRIPTION

The RNA Clean & Concentrator kits are RNA clean up kits that provide a simple and reliable method for the rapid preparation of high-quality RT-PCR-ready, DNA-free (R1013, R1014) RNA. This simple procedure is based on the use of a unique single-buffer system and Zymo-Spin column technology that allows for selective recovery of total RNA (> 17 nt), large RNAs (> 200 nt), and/or small RNAs (17-200 nt). The procedure is easy: Add binding buffer and ethanol to your sample, then bind, wash and elute ultra pure RNA. The RNA can be eluted from the Zymo-Spin IC Column in as little as ≥ 6 µl of RNase-free water. The highly-concentrated, purified RNA is suitable for all subsequent analyses and molecular manipulations.

Learn More

Equipment	Microcentrifuge
Format	Spin-Column
Purity	RNA is ready for Next-Gen sequencing, RT-PCR, microarray, hybridization, etc. A260/A280, A260/A230: > 1.8.
Sample Source	DNase I treated RNA, in vitro transcription products, the aqueous phase following TRIzol/chloroform or similar extraction
Size Range	Total RNA ≥ 17 nt
Yield	10 µg RNA (binding capacity), ≥ 6 µl (elution volume)

Q1: Can the RCC kit be used to purify DNA (cDNA)?

Yes. The kit efficiently recovers all types of nucleic acids.

Q2: Should carrier RNA be added to the sample prior to purification?

Carrier RNA can be added with no detrimental effects. The RCC is highly efficient without the need for carrier RNA, and no significant improvement in recovery has been observed with carrier RNA.

Q3: Will this kit remove fluorescent dyes, radiolabeled dNTP’s and/or Biotin?

Yes, the kit efficiently removes unincorporated fluorescent dyes, radiolabeled dNTP’s and Biotin.

Q4: Are samples containing high concentration of detergents, salts, formamide or sucrose compatible with the RCC buffer system?

Product Tolerance Reference: – ≤5% Triton X-100 – ≤5% Tween-20 – ≤5% Sarkosyl – ≤0.1% SDS – ≤90% formamide – Sucrose samples should be diluted/titrated down 10- to 100- fold.

Q5: Can other DNase I enzymes or sets (e.g. Qiagen DNase I) be used?

Yes, follow respective protocol for on-column DNase treatment. If the DNase does not have a protocol, proceed with in-tube DNase treatment post clean-up, then re-purify.

Q6: Is DNase I treatment necessary?

If the downstream application requires DNA-free RNA, we would recommend performing in-column or in-tube DNase I treatment.

주문정보

CAT.No	품명	규격	비고
R1015	RNA Clean & Concentrator™-5	50 preps.	Format: Spin-Columns Elution Volume: ≥ 6 μl Binding Capacity: 10 μg RNA Size Limits: ≥ 17 nt Processing Time: 5 minutes
R1016	RNA Clean & Concentrator™-5	200 preps.	Format: Spin-Columns Elution Volume: ≥ 6 μl Binding Capacity: 10 μg RNA Size Limits: ≥ 17 nt Processing Time: 5 minutes
R1013	RNA Clean & Concentrator™-5 w/ DNase I	50 preps.	Format: Spin-Columns Elution Volume: ≥ 6 μl Binding Capacity: 10 μg RNA Size Limits: ≥ 17 nt Processing Time: 5 minutes
R1014	RNA Clean & Concentrator™-5 w/ DNase I	200 preps.	Format: Spin-Columns Elution Volume: ≥ 6 μl Binding Capacity: 10 μg RNA Size Limits: ≥ 17 nt Processing Time: 5 minutes