Introduction

Intended Use

For enriching bile-tolerant Gram-negative bacteria in the microbiological examination of pharmaceutical products.

Principle and Interpretation

Pancreatic digest of gelatin provide protein, vitamins and amino acids; glucose carbon source; disodium hydrogen phosphate and potassium dihydrogen phosphate as a buffer; ox bile and brilliant green as selective antibacterial agent, inhibiting the growth of non-Enterobacteriaceae.

Formulation

Ingredients	/liter
Pancreatic digest of gelatin	10g
Glucose monohydrate	5g
Dehydrated ox bile	20g
Potassium dihydrogen phosphate	2g
Disodium hydrogen phosphate dihydrate	8g
Brilliant green	15mg
pH7.2±0.2 at 25°C

Preparation

Suspend 45g in 1L of distilled water,stir until completely dissolved and dispense 100 mL into test tubes , heat at 100 °C for 30 min in a waterbath or flowing steam.

Quality Control

The following quality control strains were inoculated and cultured at 30-35℃ for 24h-48h. The results are as follows:

Quality control strains	Inoculum (CFU)	Growth
Escherichia coli ATCC8739	< 100	Good growth
Pseudomonas aeruginosa ATCC9027
Staphylococcus aureus ATCC6538	> 100	Inhibited

Storage and Shelf Life

2-30℃，Keep container tightly closed, avoid direct sunlight.

Use before expiry date on the label.

 Precautions

1. When weighing the dehydrated medium, please wear masks to avoid causing respiratory system discomfort

2. Keep container tightly closed after using to prevent clumping.

Waste Disposal

Microbiological contamination was disposed by autoclaving at 121°C for

30 minutes.

Intended Use For enriching bile-tolerant Gram-negative bacteria in the microbiological examination of pharmaceutical products. Principle and Interpretation Pancreatic digest of gelatin pro……

Introduction

This product is suitable for rapid extraction of DNA from FFPE sample. This kit uses two combination methods. High-salt Bind is conducive to remove pigments or polysaccharides from complex FFPE samples, so as to improve the purity of nucleic acid and avoid blocking aligent 2100. Alcohol mediated adsorption is conducive to improve the nucleic acid yield of high-yield samples.

Details

Specifications

Features	Specifications
Main Functions	Isolation high pure total DNA from FFPE using high bind beads
Applications	PCR and viral DNA detection, etc.
Purification technology	Magnetic beads technology
Process method	Manual or automatic
Sample type	Paraffin embedded tissue samples
Sample amount	1-6 slices of 10-20μm
Elution volume	≥30μl
Time per run	≤60 minutes

Principle

This product is based on the purification method of high binding magnetic particles. The sample is lysed and digested under the action of lysate and Protease. DNA is released into the lysate. After adding magnetic particles and binding solution, DNA will be adsorbed on the surface of magnetic particles, and impurities such as proteins will be removed without adsorption. The adsorbed particles were washed with washing solution to remove proteins and impurities, washed with ethanol to remove salts, and finally DNA was eluted by Elution Buffer.

Advantages

• High yield – most optimal process, recovery up to 90%
• Economy – less than 50% of the price of Qiagen and other imported products
• High purity – OD 260/280 : 1.7-1.9, OD 260/230 : 1.5-2.0

Kit Contents

Contents	D632301D	D632302D
Purification Times	48 Preps	96 Preps
MagPure Particles N	1.1 ml	2.5 ml
RNase A	10 mg	20 mg
Proteinase K	24 mg	48 mg
Protease Dissolve Buffer	3 ml	6 ml
Buffer DPS	60 ml	100 ml
Buffer ATL	15 ml	30 ml
Buffer BST1	30 ml	60 ml
Buffer BW1	13 ml	44 ml
Elution Buffer	15 ml	30 ml

Storage and Stability

Proteinase K, RNase A and MagPure Particles N should be stored at 2-8°C upon arrival. However, short-term storage (up to 12 weeks) at room temperature (15-25°C) does not affect their performance. The remaining kit components can be stored at room temperature (15-25°C) and are stable for at least 18 months under these conditions.

This product is suitable for rapid extraction of DNA from FFPE sample. This kit uses two combination methods. High-salt Bind is conducive to remove pigments or polysaccharides from complex FFPE samples, so as to improve the purity of nucleic acid and avoid blocking aligent 2100. Alcohol mediated adsorption is conducive to improve the nucleic acid yield of high-yield samples.

TCO-PEG4-DBCO is a heterobifunctional click chemistry reagent containing a TCO and a DBCO moiety. TCO group specifically and efficiently reacts with terrahydrazine at fast speed. DBCO is very reactive toward Azide through copper free click chemistry, the PEG spacer increases the aqueous solubility of the reagent. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.

TCO-PEG4-DBCO is a heterobifunctional click chemistry reagent containing a TCO and a DBCO moiety. TCO group specifically and efficiently reacts with terrahydrazine at fast speed. DBCO is very reactive toward Azide through copper free click chemistry, the PEG spacer increases the aqueous solubility of the reagent. Reagent grade, for research purpose. Please contact us for GMP-grade inquiries.