PlusPlasma Low Abundance Protein Enrichment and Pretreatment Kit P1456360-10T Aladdin

$559.00
In stock
SKU
P1456360-10T

Product Information

Product NamePlusPlasma Low Abundance Protein Enrichment and Pretreatment Kit
Specifications & PurityBioReagent, sterile, Proteomics grade
SynonymsLow Abundance Protein Enrichment and Pretreatment Kit

Product Description

Product Introduction:

This product is a one-stop processing kit from plasma to peptides. It utilizes nanotechnology to effectively enrich low-abundance proteins in plasma and processes plasma proteins in combination with the innovative concept of "All In One Tube". Even researchers without omics background can quickly prepare pretreated samples, which can be directly used for subsequent mass spectrometry analysis.

Product Components and Storage Conditions:

P1456360

Component

10T

25T

Storage

P1456360A

Magnetic beads

10T

25T

4℃

P1456360B

Incubation Buffer I

4.8 mL

12 mL

RT

P1456360C

Incubation Buffer II

6 mL

15 mL

RT

P1456360D

Washing Buffer

6 mL

15 mL

RT

P1456360E

Lysis Buffer

0.6 mL

1.5 mL

-20℃. Store in the dark.

P1456360F

Balance Buffer

2.8mL

7 mL

4℃

P1456360G

Digest Buffer

16 μL

40 μL

-20℃

P1456360H

Stop Buffer

300 μL

750 μL

RT

P1456360I

Wash Buffer I

4 mL

10 mL

RT

P1456360J

Wash Buffer II

2.4 mL

6 mL

RT

P1456360K

Wash Buffer III

2.4 mL

6 mL

RT

P1456360L

Elution Buffer

4.8 mL

12 mL

RT. Store in the dark.

P1456360M

Loading Buffer

120 μL

300 μL

RT

P1456360N

Tip柱

10T

25T

RT

Product Features:

Convenient and fast: The processing from plasma to peptides can be completed with one kit.

Simple operation: The instruments used are simple, requiring only a conventional centrifuge and a metal bath.

Good stability: Each batch undergoes strict quality inspection, ensuring high reproducibility of experimental results.

Operating Procedure:

1.Centrifuge the plasma sample (3000g, 10min), and take the supernatant for later use (if storage is required, store it at -80°C for long-term preservation to avoid repeated freezing and thawing).

2.Take 50-100μL of centrifuged plasma, add 400μL of Incubation buffer I, then add 30μL of Magnetic beads, vortex to mix, and incubate at room temperature on a shaking mixer for 1 hour.

3.After incubation, use a magnetic rack to magnetically separate for 3min, and discard the supernatant.

4.Remove the EP tube, add 500μL of Incubation buffer II, gently invert up and down to mix several times, magnetically separate for 3min, and discard the supernatant.

5.Remove the EP tube, add 500μL of Washing Buffer, gently invert up and down to mix several times, magnetically separate for 3min, and discard the supernatant.

6.Remove the EP tube, add 50μL of Lysis Buffer to resuspend the beads, place in a water bath at 95°C for 10min, then take it out and cool to room temperature.

7.Add 225μL of Balance buffer to the EP tube that has cooled to room temperature.

8.Add 1μL of Digest buffer to the sample, and perform enzymatic digestion with shaking in a metal bath at 37°C and 1200rpm for 3-16h.

9.After enzymat

ic digestion, take out the EP tube, add 25μL of Stop buffer to the sample, and vortex to mix.

10.Add 320μL of

Wash buffer I, shake vigorously for 3min, centrifuge at 15000rpm for 3min, and remove the upper liquid.

11.Transfer the lower layer sample into the Tip column, centrifuge at 2500rpm for 3-5min until all the liquid is centrifuged down. If the liquid flow rate is slow, the rotation speed can be appropriately increased.

12.Add 200μL of

Wash buffer II

(shake for 10-20s before use) to the desalting column, centrifuge at 2500rpm for 3-5min until all the liquid is centrifuged down.

13.Add 200μL of

Wash buffer III

to the

desalting column, centrifuge at 2500rpm for 3-5min until all the liquid is centrifuged down.

14.Put the desalting column into a new EP tube, add 200μL of Elution buffer to the desalting column, centrifuge at 2000rpm for 3-5min until all the liquid is centrifuged down.

15.Repeat the previous step, collect the eluates from both times, and freeze-dry them.

16.Add 10μL of Loading buffer, vortex vigorously for 3min, centrifuge at 2000g for 10min, take an appropriate amount of sample for mass spectrometry detection. Taking the HF-X instrument as an example, 0.5-1μg of sample is sufficient for loading.

Automated Operation Process:

It is compatible with mass spectrometry proteomics pretreatment workstations, enabling one-stop processing from plasma to peptides. This eliminates manual operation errors, improves the reproducibility of sample preparation workflows, and provides high precision and reliability for various laboratory procedures.

Storage and Shipping

Shipped InIce chest + Ice pads
Stability and StorageP1456360A、P1456360F: Store at 2-8℃ long term (12 months). P1456360E: Store at -20℃ long term (12 months). Store in the dark. P1456360G: Store at -20℃ long term (12 months). P1456360L: Store at room temperature long term (12 months). Store in the dark. P14
Storage TempStore at 2-8°C,Protected from light,Room temperature,Store at -20°C

Additional Information

SensitivityLight-sensitive

MDSD

Datasheet

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