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Key Documents

MABS1918

Sigma-Aldrich

Anti-Ubiquitin Lys6 specific Affimer reagent GFP/His tag

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About This Item

Code UNSPSC :
12352203
Nomenclature NACRES :
NA.41

Source biologique

bacterial

Niveau de qualité

Conjugué

unconjugated

Forme d'anticorps

purified antibody

Type de produit anticorps

primary antibodies

Clone

K6_29, recombinant monoclonal

Poids mol.

calculated mol wt 8.60 kDa
observed mol wt ~16 kDa

Espèces réactives

human

Conditionnement

antibody small pack of 100 μg

Technique(s)

western blot: suitable

Isotype

IgG

Conditions d'expédition

dry ice

Température de stockage

2-8°C

Modification post-traductionnelle de la cible

unmodified

Description générale

Ubiquitin (Ub), a highly conserved 76-amino acid (8.6 kDa) protein that escorts proteins for rapid degradation to the multi-component enzymatic complex known as the 26S proteasome. Ubiquitin is initially produced as polyubiquitin-B or polyubiquitin-C precursor protein and its posttranslational cleavage yield multiple copies of identical 76-amino acid ubiquitin. Ubiquitin is involved in one of the most common post-translational modifications of cellular proteins, where it is linked covalently via its carboxyl terminus (Gly76) to lysine residues in target proteins. A given target lysine residue can be linked to one single ubiquitin molecule (monoubiquitylated) or to a chain of ubiquitins (polyubiquitylated). In a polyubiquitin chain, ubiquitin molecules can be linked through one of the seven lysine residues (K6, K11, K27, K29, K33, K48, and K63) or through the ubiquitin N-terminus methionine 1 residue (which generates linear chains). Polyubiquitin chains, when attached to a target protein, have different functions depending on the Lys residue of the ubiquitin that is linked: Lysine 6-linked may be involved in DNA repair; Lysine 11-linked is involved in endoplasmic reticulum-associated degradation, lysine 29-linked is involved in lysosomal degradation, and Lysine 48-linked is involved in protein degradation via the proteasome. Affimer molecules are small proteins (~ 12 kDa) that bind to target molecules with similar specificity and affinity to that of antibodies. These engineered non-antibody binding proteins are designed to mimic the molecular recognition characteristics of monoclonal antibodies in different applications. It has been shown that each affimer molecule ca bind one ubiquitin molecule and the Affimer dimerizes to bind the two ubiquitin moieties of a diubiquitin in a linkage-specific manner. The K6 Affimer is reported to tightly bind to K6 diubiquitin in a highly specific manner. It can be used to detect K6 chains and with polyubiquitin enrichment it can detect even the endogenous levels of K6 chains. (Ref.: Michel, MA., et al. (2017). Mol. Cell. 68(1); 233-246).

Spécificité

Anti-diUbiquitin K6 GFP/His-tag Affimer reagent detects K6 linked poly-ubiquitin chains with a KD of approximately 20 pM. Binding to other di-ubiquitin linkages is negligible.

Immunogène

Ubiquitin Lys6 specific Affimer reagent, Anti-Ubiquitin Lys6 specific Affimer reagent, Ubiquitin Lys6 specific Affimer Reagent GFP/His tag

Application

Quality Control Testing

Evaluated by Western Blotting with Various K-linked di-ubiquitin chains.

Western Blotting Analysis (WB): A 1:1,000 dilution of this Affimer reagent detected di-ubiquitin K6-linkages.

Tested Applications

Western Blotting Analysis: A representative lot of this Affimer detected di-Ubiquitin Lys6. in Western Blotting applications (Michel, M.A., et. al. (2017). Mol Cell. 68(1):233-246).

Note: Actual optimal working dilutions must be determined by end user as specimens, and experimental conditions may vary with the end user
Anti-Ubiquitin Lys6 specific GFP/His-tag Affimer reagent, Cat. No. MABS1918, detects diubiquitin K6-linkage and is tested for use in Western Blotting.

Forme physique

Purified GFP/His-tag Affimer reagent in buffer containing 100 mM Sodium Phosphate, 150 mM Sodium Chloride, 0.02% Sodium Azide, pH 7.4.

Stockage et stabilité

Recommend storage at +2°C to +8°C. For long term storage antibodies can be kept at -20°C. Avoid repeated freeze-thaws.

Autres remarques

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Clause de non-responsabilité

Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.

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Code de la classe de stockage

12 - Non Combustible Liquids

Classe de danger pour l'eau (WGK)

WGK 2

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


Certificats d'analyse (COA)

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