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5 mL 1 μm Magnetic Beads Dna Library Construction Kit Oligo dT Bind mRNA Poly A

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5 mL 1 μm Magnetic Beads Dna Library Construction Kit Oligo dT Bind mRNA Poly A
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Features
Specifications
Product Name: Oligo DT Magbeads
Storage: Stored At 2 ~ 8 ℃, Avoid Freezing
Package: 1ml/2ml/5ml
Method Base: Magnetic Beads Method
Application: PCR Amplification, Sequencing And Detection.
Concentration: 5 Mg/mL
Product Number: 70431-5
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1 um Dna Library Construction Kit

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oligo dt magnetic beads mRNA

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Medium Bottle Dna Library Construction Kit

Basic Infomation
Place of Origin: China
Brand Name: BeaverBeads
Certification: COA
Model Number: 5 mL
Payment & Shipping Terms
Packaging Details: 1ml/2ml/5ml
Delivery Time: 5-8 days
Payment Terms: T/T, L/C
Supply Ability: 850 L/month
Product Description

Magbeads coupled with Oligo dT capture high quality mRNA

 

1, Description

BeaverBeadsTM Oligo dT applying surface covalently conjugated with Oligo dT, can couple with Poly A at the tail of mRNA in eukaryotes. BeaverBeadsTM Oligo dT can efficiently separate complete and high purity mRNA from eukaryotic total RNA, animal and plant tissues or cell lysates. The isolated mRNA can be used in various molecular biological experiments: RT-PCR, solid phase cDNA library construction, RACE, Northern, etc.

 

2, Product Information

Product Name BeaverBeads™ Oligo dT
Bead Size 1 μm
Oligo dT (pmol/mg bead) 500
mRNA Binding Ability (μg/mg bead) 1-2
Concentration (mg/mL) 5
Preservation Solution 1×PBS,0.1%(v/v)proclin-300
Shelf Life 2~8℃, 2 years
Applicable Sample Type Total RNA, crude cell samples, animal tissue, plant tissue, etc.

 

 

3, Features

1. High purity: The recovered product can be directly used for second generation sequencing (NGS) database construction;
2. Precise screening: free selection of screening ranges for nucleic acid fragments and accurate screening;
3. Good operating performance: The magnetic beads have fast magnetic response, which effectively prevents the effects caused by the residual magnetic beads.

 

4, Product Advantages

1. Abundant surface active sites and high mRNA capture efficiency;

2. Low nonspecific adsorption and high mRNA purity;

3. Uniform particle size, good suspension, and low sedimentation rate;

4. Short magnetic response time, suitable for automatic operation;

5. Industrial scale production, high batch stability.

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