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SAB4200082

Sigma-Aldrich

Monoclonal Anti-Maltose Binding Protein (MBP) antibody produced in rat

1.0 mg/mL, clone MBP 7G4, purified immunoglobulin

Synonyme(s) :

Anti-MBP

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About This Item

Numéro MDL:
Code UNSPSC :
12352203
Nomenclature NACRES :
NA.56

Source biologique

rat

Niveau de qualité

Conjugué

unconjugated

Forme d'anticorps

purified immunoglobulin

Type de produit anticorps

primary antibodies

Clone

MBP 7G4, monoclonal

Forme

buffered aqueous solution

Poids mol.

antigen ~42 kDa

Espèces réactives

wide range

Concentration

1.0 mg/mL

Technique(s)

immunoprecipitation (IP): suitable
indirect ELISA: suitable
western blot: 0.1-0.2 μg/mL using MBP recombinant protein

Isotype

IgG2a

Conditions d'expédition

dry ice

Température de stockage

−20°C

Modification post-traductionnelle de la cible

unmodified

Description générale

MBP is part of a large class of proteins that aid in the uptake of small molecules. While it naturally resides in the periplasm, MBP can also be expressed at high yields in the cytoplasm. For different proteins, increased solubility, enhanced stability and markedly improved yields have been reported after fusion to MBP.
Monoclonal Anti-Maltose Binding Protein (MBP) (rat IgG2a isotype) is derived from the hybridoma MBP 7G4 produced by the fusion of mouse myeloma cells (P3X63Ag8.653) and splenocytes from rat immunized with MBP-fusion protein.1 The antibody is purified from culture supernatant of hybridoma cells grown in a bioreactor. Monoclonal Anti- Maltose Binding Protein (MBP) is specific for MBP.

Spécificité

Monoclonal Anti- Maltose Binding Protein (MBP) is specific for MBP.

Immunogène

MBP-fusion protein

Application

Monoclonal Anti-Maltose Binding Protein (MBP) antibody produced in rat is suitable for:
  • immunoblotting
  • enzyme linked immunosorbent assay (ELISA)
  • immunoprecipitation

Monoclonal antibodies recognizing specifically MBP are useful in various immunotechniques for identifying the expression of an MBP fusion protein in bacteria or in cells transfected with MBP fusion protein expressing vectors.

Actions biochimiques/physiologiques

Maltose binding protein (MBP) tag is known to be used in genetic engineering to create a stable fusion product that does not appear to interfere with the bioactivity of the protein of interest or with the biodistribution of the MBP tagged product. The expression of polypeptides in-frame with maltose binding protein (MBP) allows for their easy purification from bacterial extracts under mild conditions, which employ a single affinity chromatographic step on amylose resin. This system and others based on the expression of fusion proteins utilize a specific protease cleaving site to facilitate correct cleavage of the fusion protein. Thus, the MBP system incorporates a factor Xa cleavage site at the carboxy terminus of the MBP sequence, and cleavage by factor Xa separates MBP from its partner protein. Many recombinant proteins have been engineered with MBP tags to facilitate the detection, isolation and purification of the proteins.

Forme physique

Solution in 0.01M phosphate buffered saline pH 7.4, containing 15 mM sodium azide.

Stockage et stabilité

Store at -20 °C. For continuous use, the product may be stored at 2-8 °C for up to one month. For extended use, freeze at -20 °Cin working aliquots. Repeated freezing and thawing, or storage in “frost-free” freezers, is not recommended. If slight turbidity occurs upon prolonged storage, clarify by centrifugation. Working dilution samples should be discarded if not used within 12 hours.

Clause de non-responsabilité

Unless otherwise stated in our catalog, 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

10 - Combustible liquids

Point d'éclair (°F)

Not applicable

Point d'éclair (°C)

Not applicable


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Consulter la Bibliothèque de documents

José J Rodríguez-Herva et al.
Cellular microbiology, 14(5), 669-681 (2012-01-12)
The bacterial pathogen Pseudomonas syringae pv tomato DC3000 suppresses plant innate immunity with effector proteins injected by a type III secretion system (T3SS). The cysteine protease effector HopN1, which reduces the ability of DC3000 to elicit programmed cell death in
Fusion tags for protein solubility, purification and immunogenicity in Escherichia coli: the novel Fh8 system
Costa S, et al.
Frontiers in Microbiology, 5, 63-63 (2014)
A bacterial cysteine protease effector protein interferes with photosynthesis to suppress plant innate immune responses
Rodriguez HJ, et al.
Cellular Microbiology, 14(5), 669 ?681-669 ?681 (2016)
Comparative analyses of ubiquitin-like ATG8 and cysteine protease ATG4 autophagy genes in the plant lineage and cross-kingdom processing of ATG8 by ATG4
Seo E, et al.
Autophagy, 12(11), 2054-2068 (2016)
T Ikeda et al.
Gan to kagaku ryoho. Cancer & chemotherapy, 13(4 Pt 1), 1044-1049 (1986-04-01)
A study of postoperative adjuvant chemotherapy according to cell type, combined with immunotherapy using PSK and OK-432 was conducted in 178 lung cancer patients who had undergone resection. BRM (PSK or OK-432) was selected by randomization. Chemotherapy was mainly performed

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