Alexa Fluor™ 488 Microscale Protein Labeling Kit
Now available:Upgraded Alexa Fluor Antibody Labeling kits with user-friendly, advanced purification columns that ensure rapid dye removal and high yield of labeled proteins in just 30 minutes, with minimal hands-on time.
Alexa Fluor™ 488 Microscale Protein Labeling Kit
Invitrogen™

Alexa Fluor™ 488 Microscale Protein Labeling Kit

Microscale Protein Labeling Kits provide a convenient means for attaching a fluorescent label to a small amount of antibody or深入閱讀
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產品號碼Quantity
A300061 Kit
產品號碼 A30006
價格 (TWD)
21,980.00
Online offer
Ends: 31-Dec-2025
31,400.00
您節省 9,420.00 (30%)
Each
新增至購物車
Quantity:
1 Kit
價格 (TWD)
21,980.00
Online offer
Ends: 31-Dec-2025
31,400.00
您節省 9,420.00 (30%)
Each
新增至購物車

Microscale Protein Labeling Kits provide a convenient means for attaching a fluorescent label to a small amount of antibody or protein (20–100 μg). The kits are available in four Alexa Fluor™ colors (or biotin) and supply everything needed for three labeling and separation reactions.

Important Features of Microscale Protein Labeling Kits:

  • Labeled proteins typically ready to use typically in 2 hr (∼30 min hands-on time)
  • Optimized for 20–100 μg of protein with molecular weights between 12 and 150 kDa
  • Purified using convenient spin filters with yields between 60 and 90%
  • Stabilizing proteins must be removed from the sample before labeling

Stable Reaction Chemistry and Superior Alexa Fluor™ Dyes

In the Microscale Protein Labeling Kits, the reactive dye contains a tetrafluorophenyl (TFP) ester moiety that is more stable in solution than the commonly used succinimidyl (NHS) ester. TFP esters react efficiently with primary amines of proteins to form stable dye–protein conjugates. Compared to traditional dyes, Alexa Fluor™ dyes are brighter, more photostable, and more pH resistant between pH 4 and 10. And generally when using Alexa Fluor™ dyes, higher degrees of labeling can be achieved without intramolecular quenching. For details see Alexa Fluor™ Dyes Spanning the Visible and Infrared Spectrum—Section 1.3.

Learn More About Protein and Antibody Labeling

We offer a wide selection of Molecular Probes™ antibody and protein labeling kits to fit your starting material and your experimental setup. See Antibody Labeling from A to Z or use our Labeling Chemistry Selection Tool for other choices. To learn more about our various kits read Kits for Labeling Proteins and Nucleic Acids—Section 1.2 in the Molecular Probes™ Handbook.

We'll Make a Custom Antibody Conjugate for You

If you can't find what you're looking for in our stocked list, we'll prepare a custom antibody conjugate for you. Our custom conjugation service is efficient and confidential, and we stand by the quality of our work. We are ISO 13485:2000 certified.

For Research Use Only. Not for use in diagnostic procedures.
規格
ColorGreen
Detection MethodFluorescence
Excitation/Emission495/519 nm
Label TypeAlexa Fluor
Labeling MethodConjugation-based
Labeling Scale20–100 μg
Product LineAlexa Fluor
Product TypeLabeling Kit
Quantity1 Kit
Reactive MoietyTetrafluorophenyl (TFP) Ester
Shipping ConditionRoom Temperature
Labeling TargetProteins
Label or DyeAlexa Fluor 488
Unit SizeEach
內容物與存放
Store in refrigerator 2°C to 8°C and protect from light.

常見問答集 (常見問題)

Can I use 50 μg of protein with Fluorescent Protein Labeling Kits?

No. We recommend using 1 mg of protein with Fluorescent Protein Labeling Kits. For smaller protein sample sizes, we recommend using Microscale Protein Labeling kits which are optimized for 20-100 µg of protein.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

What formulation of antibody should I use for conjugation for small animal in vivo imaging?

To allow for good reaction kinetics, antibodies should be in PBS buffer at a concentration of 0.5-3.0 mg/ml. The antibody must be free of preservatives (azide etc.), amine containing buffers and carrier proteins such as BSA.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

What is degree of labeling (DOL)?

Degree of labeling (DOL) describes the number of fluorophores per antibody. For in vivo labeling experiments, the DOL is restricted to a narrow range because it has significant consequences for the biodistribution and clearance of the probe. For example, for in vivo imaging, we have determined that the DOL range for the far-red Alexa Fluor dyes is 1.5 to 3 molecules per antibody for optimal optical in vivo imaging.

Find additional tips, troubleshooting help, and resources within our Cell Analysis Support Center.

引用資料與參考文獻 (68)

引用資料與參考文獻
Abstract
Golgi apparatus immunolocalization of endomannosidase suggests post-endoplasmic reticulum glucose trimming: implications for quality control.
Authors:Zuber C, Spiro MJ, Guhl B, Spiro RG, Roth J
Journal:Mol Biol Cell
PubMed ID:11102520
'Trimming of N-linked oligosaccharides by endoplasmic reticulum (ER) glucosidase II is implicated in quality control of protein folding. An alternate glucosidase II-independent deglucosylation pathway exists, in which endo-alpha-mannosidase cleaves internally the glucose-substituted mannose residue of oligosaccharides. By immunogold labeling, we detected most endomannosidase in cis/medial Golgi cisternae (83.8% of immunogold ... More
Glycosylation influences the lectin activities of the macrophage mannose receptor.
Authors:Su Y, Bakker T, Harris J, Tsang C, Brown GD, Wormald MR, Gordon S, Dwek RA, Rudd PM, Martinez-Pomares L
Journal:J Biol Chem
PubMed ID:15983039
'The mannose receptor (MR) is a heavily glycosylated endocytic receptor that recognizes both mannosylated and sulfated ligands through its C-type lectin domains and cysteine-rich (CR) domain, respectively. Differential binding properties have been described for MR isolated from different sources, and we hypothesized that this could be due to altered glycosylation. ... More
An endocytosed TGN38 chimeric protein is delivered to the TGN after trafficking through the endocytic recycling compartment in CHO cells.
Authors:Ghosh RN, Mallet WG, Soe TT, McGraw TE, Maxfield FR
Journal:J Cell Biol
PubMed ID:9722606
'To examine TGN38 trafficking from the cell surface to the TGN, CHO cells were stably transfected with a chimeric transmembrane protein, TacTGN38. We used fluorescent and 125I-labeled anti-Tac IgG and Fab fragments to follow TacTGN38''s postendocytic trafficking. At steady-state, anti-Tac was mainly in the TGN, but shortly after endocytosis it ... More
Alexa dyes, a series of new fluorescent dyes that yield exceptionally bright, photostable conjugates.
Authors:Panchuk-Voloshina N, Haugland RP, Bishop-Stewart J, Bhalgat MK, Millard PJ, Mao F, Leung WY, Haugland RP
Journal:J Histochem Cytochem
PubMed ID:10449539
'Alexa 350, Alexa 430, Alexa 488, Alexa 532, Alexa 546, Alexa 568, and Alexa 594 dyes are a new series of fluorescent dyes with emission/excitation spectra similar to those of AMCA, Lucifer Yellow, fluorescein, rhodamine 6G, tetramethylrhodamine or Cy3, lissamine rhodamine B, and Texas Red, respectively (the numbers in the ... More
Removal of the membrane-anchoring domain of epidermal growth factor leads to intracrine signaling and disruption of mammary epithelial cell organization.
Authors:Wiley HS, Woolf MF, Opresko LK, Burke PM, Will B, Morgan JR, Lauffenburger DA
Journal:J Cell Biol
PubMed ID:9832559
'Autocrine EGF-receptor (EGFR) ligands are normally made as membrane-anchored precursors that are proteolytically processed to yield mature, soluble peptides. To explore the function of the membrane-anchoring domain of EGF, we expressed artificial EGF genes either with or without this structure in human mammary epithelial cells (HMEC). These cells require activation ... More