Anticorps Recombinant de lapin anti-MYC tag

MYC tag Recombinant Antibody for WB, IF/ICC, FC (Intra), IP, Indirect ELISA

Hôte / Isotype

Lapin / IgG

Réactivité testée

Protéine recombinante

Applications

WB, IF/ICC, FC (Intra), IP, Indirect ELISA

Conjugaison

Non conjugué

CloneNo.

241611D1

N° de cat : 80469-2-PBS

Synonymes

241611D1

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Galerie de données de validation

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  WB analysis of Transfected HEK-293T using 80469-2-RR (same clone as 80469-2-PBS)

  Transfected HEK-293T cells were subjected to SDS PAGE followed by western blot with 80469-2-RR (MYC tag antibody) at dilution of 1:50000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 80469-2-PBS in a different storage buffer formulation.

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  IP experiment of Transfected HEK-293 using 80469-2-RR (same clone as 80469-2-PBS)

  IP result of anti-MYC tag (IP:80469-2-RR, 4ug; Detection:80469-2-RR 1:5000) with Transfected HEK-293 cells lysate 1600 ug. This data was developed using the same antibody clone with 80469-2-PBS in a different storage buffer formulation.

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  IF Staining of Transfected HEK-293 using 80469-2-RR (same clone as 80469-2-PBS)

  Immunofluorescent analysis of (4% PFA) fixed Transfected HEK-293 cells using MYC tag antibody (80469-2-RR, Clone: 241611D1 ) at dilution of 1:250 and CoraLite®488-Conjugated Goat Anti-Rabbit IgG(H+L) (SA00013-2). This data was developed using the same antibody clone with 80469-2-PBS in a different storage buffer formulation.

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  FC experiment of Transfected HEK-293 using 80469-2-RR (same clone as 80469-2-PBS)

  1x10^6 Transfected HEK-293 cells were intracellularly stained with 0.25 ug MYC tag Recombinant antibody (80469-2-RR, Clone:241611D1) and CoraLite®488-Conjugated Goat Anti-Rabbit IgG(H+L) (SA00013-2), and 0.25 ug Rabbit IgG Isotype Control RecAb (98136-1-RR, Clone: 240953C9). Cells were fixed with 4% PFA and permeabilized with Flow Cytometry Perm Buffer (PF00011-C). This data was developed using the same antibody clone with 80469-2-PBS in a different storage buffer formulation.

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  Affinity and Kinetic Characterization of 80469-2-RR

  Biolayer interferometry (BLl) kinetic assays of 80469-2-RR against MYC tag were performed. The affinity constant is 0.134 nM.

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Informations sur le produit

80469-2-PBS cible MYC tag dans les applications de WB, IF/ICC, FC (Intra), IP, Indirect ELISA et montre une réactivité avec des échantillons Protéine recombinante

• Réactivité: Protéine recombinante
• Hôte / Isotype: Lapin / IgG
• Clonalité: Recombinant
• Type: Anticorps
• Immunogène: MYC tag Protéine recombinante Ag9409
• Nom complet: Myc tag
• Symbole du gène: Myc tag
• Identification du gène (NCBI): 99
• Conjugaison: Non conjugué
• Forme: Liquide
• Méthode de purification: Protein A purfication
• Tampon de stockage: PBS only
• Conditions de stockage: Store at -80°C. 20ul contiennent 0,1% de BSA.

Informations générales

The myc-tag is a short synthetic polypeptide sequence derived from c-MYC protein that can be added to recombinant proteins to enable isolation and study when an antibody is not available. This antibody recognizes the MYC tag EQKLISEEDL. MYC tag is a part of c-MYC protein. So there's weaker 62-65 kDa bands for endogenous c-MYC protein. What is the molecular weight of myc? 1203Da: the ten amino acid myc tag sequence is EQKLISEEDL (in single letter code). What are the applications for myc tag? The addition of the myc tag to a particular protein can be useful when an antibody is not available to the protein of interest. Using recombinant DNA technology, the myc tag can be fused to the protein and then an antibody against the myc tag can be used to probe (PMID: 24490106). This is a reliable method and can be used in a number of different techniques, including purification using chromatography, tracking the protein in localization studies using immunofluorescence, or quantifying levels using Western Blot (PMID: 24490106). What is the structure of myc tag? The c-myc gene from which this tag is derived has a molecular weight of 49kDa, but the myc tag represents only a small portion of the C-terminus of this gene. The short polypeptide sequence can be fused to the N-terminus or the C-terminus of any protein without influencing function, although it is advised to avoid fusing it to a secretory signal. A cleavage site behind this tag is also sometimes engineered to allow removal with a specific protease.

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