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FITC Labeling Kit (AKES145)

SKU:
AKES145
$323

Description

system_update_altDatasheetsystem_update_altMSDS
Product Name:FITC Labeling Kit
SKU:AKES145
Labeling group:FITC
Applications:Protein labeling/Antibody labeling (50 KD Filtration tube)

FITC Labeling Kit provides all the reagents required for labeling, which can label antibodies and other proteins containing primary amino-group (-NH2) molecules simply and effectively.

AKES145
Products1 Reaction3 Reactions10 ReactionsStorage
AF 568 NHS ester0.12 mg×10.12 mg×30.12 mg×1020°C, shading light
Labeling Buffer II10 mL20 mL20 mL x 22-8°C
DMF500 uL500 uL500 uL2-8°C, shading light
1×PBS(pH7.4)10 mL10 mL10 mL x 22-8°C
1M Tris(pH 8.7)500 uL500 uL500 uL x 22-8°C
3 KD Filtration tube*1 set**3 sets10 setsRT

Material Required

  • Pipettor and tips (0.5-10μL, 2-20μL, 20-200μL, 200-1000μL).
  • Ultraviolet spectrophotometer or nanodrop or multifunctional microplate reader.
  • 37°C incubator.
  • Centrifuge (centrifugal force up to 12,000×g).
AKES145

Within a certain pH range, FITC specifically reacts with primary amino groups (N-terminal and lysine residue side chains) to form a stable thiourea bond, so as to realize the coupling of FITC with protein.

AKES145
Concentration & buffer exchange:Put the filter device in the collection tube, add 1 mg of protein to be labeled into the filter device, add Labeling Buffer III to the final volume of 5 mL, cover the filter tube, centrifuge at 12,000×g for 5 min, and discard the liquid in the collection tube.
Note:The maximum volume of the filter device is 5 mLIf the volume of 1 mg protein is greater than 5 mL, please add it in several times and concentrate it by centrifugation and ultrafiltrationIf the protein to be labeled contains free amino groups (Tris, amino acids or other interferents, repeat ultrafiltration with Labeling Buffer III to ensure that it is removed full.
Recovery & quantification:Invert the filter device into the collection tube, centrifuge at 1000×g for 2 min, collect the protein in the collection tube, take out the filter device, add an appropriate amount of Labeling Buffer III into the collection tube, make sure that the protein concentration is about 2 mg/mL. At the same time, add 5 mL Labeling Buffer III into the filter device and put it on a pipe rack for later use.
Labeling reaction:Immediately add 3 μL of 7 mM FITC to the protein solution, gently blow and mix fully, sealed with a lid, and incubate at 37°C for 30 min in the dark.
Ultrafiltration & purification:Add an appropriate amount of 1×PBS into the above reaction solution to the final volume of 5 mL, gently mix and transfer the reaction solution to the filter device, make sure that the Labeling Buffer III in the filter device in step 2 should be discard (if the above reaction solution exceeds 5 mL, it can be transferred to the spin-dried filter device for several times after ultrafiltratio, and cover the cap after matching with the collection tube, and centrifuge for 5~10 min at the speed of 12,000×g. Discard the liquid in the collection tube, replenish 5 1×PBS to 500 μL in the filter device, and repeat the centrifugal ultrafiltration operation for 2~3 times until the color of the ultrafiltrate in the collection tube is almost colorless and transparent.
Collect labeled product:Add 2 mL 1×PBS into the filter device and pipet gently. Invert the filter device in another collection tube and centrifuge at 1000×g for 2 min. Collect the solution in the collection tube, which is the protein labeled by FITC. (OptionaDetermining the degree of labeling Use an absorbing light scanning device to set the scanning range of 230 nm~800 nm. Set 1×PBS to as blank control. Take 2 μL FITC labeled sample, scan the absorption spectrum (230 nm to 800 nand record A280 and A494 data (1 cm optical pat.
Note:In this case, it is necessary to scan the absorption value in the range of 230nm~800nm, rather than measuring the value at A280 and ABy observing the absorption spectrum curve, some abnormal values can be eliminated, such as the measurement error caused by bubbles in the sampleThe DOS and protein concentration can be calculated based on the molar extinction coefficient of FITC dye, the A280 correction value, the molar extinction coefficient of the protein, the molecular weight of the protein, etcThe calculation formula is as follows: DOS = (A494×εIgG)/( εFITC×(A280-CF280×A494)) Protein concentration (mg/mL)=(A280-CF280×AFITC)×150000/εIgG 6
Storage:2~8°C/-20°C, shading light
Expiration date:12 months
Shipping:Ice bag

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