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MilliporeSigma

FITC1

FluoroTag FITC Conjugation Kit

Synonym(s):

FITC

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1 KIT

$496.00

$496.00


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About This Item

NACRES:
NA.32
UNSPSC Code:
12352200

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packaging

pkg of (Kit contains reagents for 5 conjugations.)

fluorescence

λex 495 nm; λem 525 nm

storage temp.

2-8°C

Quality Level

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This Item
APOAFSBR00028SAB3700992
packaging

pkg of (Kit contains reagents for 5 conjugations.)

packaging

pkg of 1 kit

packaging

-

packaging

-

fluorescence

λex 495 nm; λem 525 nm

fluorescence

-

fluorescence

-

fluorescence

-

storage temp.

2-8°C

storage temp.

2-8°C

storage temp.

−20°C

storage temp.

2-8°C

Quality Level

200

Quality Level

300

Quality Level

100

Quality Level

100

Application

The Flourotag FITC Conjugation Kit can be used for Immunohistochemisty and Immunocytochemistry using Flow Cytometry. It is also be used for the conjugation of FITC to peptide hormones, cytokines, growth factors and proteins.

Biochem/physiol Actions

Sigma offers a convenient kit for preparing FITC-labeled antibodies. Fluorescein isothiocyanate (FITC), Isomer 1, is a widely used fluorophore, popular because of its high quantum efficiency and stability when conjugated. FITC is yellow-orange in color with an absorption maximum at 495 nm. Upon excitation it emits a yellow-green color with an emission maximum at 525 nm. Conjugation occurs through free amino groups of proteins or peptides, forming a stable thiourea bond (see reaction). FITC conjugates of antibodies, lectins, hormones, and growth factors have been used in a variety of immunohistochemical and flow cytometry applications. The protocols have been optimized for antibodies, but may be adapted to other proteins by the end user.

Features and Benefits

  • Suitable for both small (1 mg) and large (5 mg) scale conjugations
  • Completely aqueous procedure - no DMF needed
  • Fast gel filtration separation of conjugate from excess FITC
  • Complete protocols for conjugation and F/P ratio determination
  • Sufficient reagents for at least 5 conjugations of 5 mg protein each and for optimization of F/P ratio before scale-up
  • References for applications and protocols

Analysis Note

Procedure
1. Dissolve protein and FITC in carbonate-bicarbonate buffer.
2. Slowly add FITC to protein with stirring. Cover with foil and stir 2 hours at room temperature.
3. Separate conjugate from free FITC on G-25 column. Collect fractions.
4. Pool fractions containing conjugate.
5. Determine F/P ratio of conjugate spectrophotometrically.
6. Stabilize with 1% bovine serum albumin and 0.1% sodium azide and store at 0-5 °C.

Legal Information

FluoroTag is a trademark of Sigma-Aldrich Co. LLC

Kit Components Only

Product No.
Description

  • Sephadex G-25 column, 3.5 mL 1

  • Sephadex G-25 column, 9.1 mL 1

  • Fluorescein isothiocyanate isomer I - F7250KC-2MG 2 mg

Kit Components Also Available Separately

Product No.
Description
SDS

  • P3813Phosphate buffered saline, powder, pH 7.4, for preparing 1 L solutions 5 pkgSDS

related product

pictograms

Exclamation mark

signalword

Warning

hcodes

Hazard Classifications

Eye Irrit. 2

Storage Class

10 - Combustible liquids

flash_point_f

Not applicable

flash_point_c

Not applicable


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H Hidaka et al.
Journal of lipid research, 40(6), 1131-1139 (1999-06-05)
We previously reported the identity and purification of two HDL3-binding proteins in rat liver plasma membranes. As these proteins are candidate high density lipoprotein (HDL) receptors and probably multifunctional, including a role in HDL metabolism, we have considerable interest in
P F Blackmore
Steroids, 64(1-2), 149-156 (1999-05-14)
Progesterone rapidly increased intracellular free calcium ([Ca2+]i) in human sperm, removal of extracellular Ca2+ prevented the increase in [Ca2+]i. The Ca2+ influx was not blocked by the T-type Ca2+ channel blocker mibefradil. However T-type calcium channels do appear to be
R F Mullins et al.
Ophthalmology, 104(2), 288-294 (1997-02-01)
Drusen are extracellular deposits that accumulate between the basal lamina of the retinal pigment epithelium and the elastic lamina of Bruch membrane in aging human eyes. Although specific types of drusen are recognized as significant risk factors for the development
Sunali Bhatnagar et al.
Journal of controlled release : official journal of the Controlled Release Society, 238, 22-30 (2016-07-16)
Inertial cavitation mediated by ultrasound has been previously shown to enable skin permeabilisation for transdermal drug and vaccine delivery, by sequentially applying the ultrasound then the therapeutic in liquid form on the skin surface. Using a novel hydrogel dosage form
Y Kobayashi et al.
Molecular human reproduction, 3(2), 91-99 (1997-02-01)
Leiomyomas are tumours of uterine smooth muscle tissue that are oestrogen and progesterone dependent. When explants of these tumours were grown in culture, the proliferating tissue formed characteristic ball-like aggregates (BLA), rather than the usual hill and valley (HV) pattern

Questions

1–6 of 6 Questions  
  1. I would like to inquire about the sensitivity, limit of detection (LOD), and limit of quantification (LOQ) for the FluoroTag™ FITC Conjugation Kit. Thank you.

    1 answer
    1. Conjugation with FITC occurs through free amino groups of proteins or peptides. The F/P molar ratio of the conjugate, as well as the limit of detection, will vary from one protein to another and must be determined empirically by the end user. Please access the Product Information Sheet in the DOCUMENTATION section of the Product Detail Page under the 'Product Information Sheet' tab for further details.

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  2. What is the Department of Transportation shipping information for this product?

    1 answer
    1. Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.

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  3. Can the columns in Product FITC1, FluoroTag™ FITC Conjugation Kit, be reused?

    1 answer
    1. Wash the column with 35 ml (10 X column volumes) of PBS to remove unbound fluorophore. This is sufficient to regenerate the column.  For prolonged storage, wash the column with 10 mL of PBS containing 0.05% sodium azide and store capped at 2-8 °C, with about 1 mL buffer above the gel.

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  4. When using Product FITC1, FluoroTag™ FITC Conjugation Kit, should I adjust the dye:protein ratio for the size of the protein being labeled?

    1 answer
    1. Adjustments for dye/protein ratios should only be made for very small proteins, i.e. < 25 kDa. Here, you should use less protein per dye portion. In many cases, this weight amount of protein is IgG with MW 150 kDa, and the kit would provide a molar excess of dye to provide attachment of a few dyes per IgG. If one wants to attempt labeling of a very small protein using the same weight ratio, there is a good chance there would not be enough dye/protein.

      Helpful?

  5. Can Product FITC1, FluoroTag™ FITC Conjugation Kit, be used with antibodies at concentrations less than 5 mg/mL?

    1 answer
    1. You can scale down the reaction for labeling.  A possible problem occurs in using the column to remove the free FITC.  If the volume is too small, the column cannot be used.  We would recommend using dialysis to remove the free (unconjugated) FITC.

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  6. My antibody is in solution containing azide.  Can I use the antibody directly in the reaction when using Product FITC1, FluoroTag™ FITC Conjugation Kit?

    1 answer
    1. It is not recommended to have azide in the reaction mix. If the buffer contains amines or sodium azide, dialyze protein solution (1 mL) against PBS, pH 7.4 (approximately 1000 mL), overnight at 2-8 °C.

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