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<M2350> Mag-Bind Bacterial DNA 96 Kit 磁珠法細菌DNA提取試劑盒

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The Mag-BIND? Bacterial DNA 96 Kit allows rapid and reliable isolation of high-quality genomic DNA (gDNA) from a wide variety of bacterial species.

磁珠法細菌DNA提取試劑盒

Mag-Bind Bacterial DNA 96 Kit


產品編號

產品名稱

包裝規格

目錄價

M2350-00

    磁珠法細菌DNA提取試劑盒      

1 x 96

2001

M2350-01

磁珠法細菌DNA提取試劑盒  

4 x 96

6850

M2350-02

磁珠法細菌DNA提取試劑盒  

20 x 96

29610


產品介紹

The Mag-BIND? Bacterial DNA 96 Kit allows rapid and reliable isolation of high-quality genomic DNA (gDNA) from a wide variety of bacterial species. Up to 0.5 mL gram positive or gram negative bacterial culture can be processed each time. The key to the system is Omega Bio-tek’s proprietary Mag-BIND? particles that avidly, but reversibly, binds DNA or RNA under certain optimal conditions allowing proteins and other contaminants to be removed. After bacterial cells are collected from culture or picked from an agar plate, the bacterial cell wall is removed by lysozyme digestion, followed by Proteinase K digestion. Following lysis, binding conditions are adjusted and the sample is mixed with Mag-BIND particles to bind DNA. Three rapid wash steps remove trace salts and protein contaminants, and finally, DNA is eluted in water or low ionic strength buffer. Purified DNA can be directly used in downstream applications without the need for further purification.



參數

FEATURES

SPECIFICATIONS

Starting Amount

0.5 mL

Starting Material

Wide variety of bacterial species

Elution Volume

200 μL

Technology

Magnetic beads

Processing Mode

Automated, Manual

Throughput

96

Note

CH beads


組分

Product

M2350-00

M2350-01

Purifications

1 × 96 preps

4 × 96 preps

Mag-Bind? Particles CH

1.1 mL

4.2 mL

MB1 Buffer

25 mL

100 mL

DS Buffer

3 mL

12 mL

MSL Buffer

25 mL

100 mL

SPM Buffer

30 mL

2 × 75 mL

Elution Buffer

30 mL

125 mL

Lysozyme

120 mg

480 mg

Proteinase K Solution

2.5 mL

10 mL

RNase A

550 μL

2.2 mL

User Manual

?

?


流程

  1. Harvest bacterial culture

  2. Lyse cells with lysozyme

  3. Transfer supernatant and bind nucleic acids to magnetic beads

  4. Concentrate magnetic beads

  5. Wash and dry

  6. Elute

  7. Concentrate beads and transfer eluate