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Merck
CN

M6295

Monoclonal Anti-Maltose Binding Protein antibody produced in mouse

clone MBP-17, ascites fluid

别名:

Monoclonal Anti-Maltose Binding Protein, Maltose Binding Protein Antibody, Maltose Binding Protein Antibody - Monoclonal Anti-Maltose Binding Protein antibody produced in mouse, Anti-MBP

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关于此项目

NACRES:
NA.46
UNSPSC Code:
12352203
Conjugate:
unconjugated
Clone:
MBP-17, monoclonal
Application:
DB, ELISA (i), WB
Citations:
20
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biological source

mouse

conjugate

unconjugated

antibody form

ascites fluid

antibody product type

primary antibodies

clone

MBP-17, monoclonal

contains

15 mM sodium azide

technique(s)

dot blot: suitable, indirect ELISA: suitable, western blot: 1:4,000 using purified, recombinant MBP

isotype

IgG1

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Quality Level

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General description

Maltose Binding Protein (MBP) is a periplasmic protein specific to bacteria. It has maltodextrin binding site and binds to linear and cyclic maltodextrins. The mature MBP is synthesized from the pre-protein comprising of 26 amino acids, as signal peptide.
The antibody recognizes native as well as denatured-reduced forms of purified MBP and MBP fusion proteins.

Immunogen

Purified, recombinant MBP fusion protein

Application

Endogenous intracellular levels of MBP in salmonella cells were determined by western blot analysis using a monoclonal anti-MBP antibody.
Monoclonal Anti-Maltose Binding Protein antibody produced in mouse has been used in the detection of MBP fusion protein using:
  • western blotting and in vitro pull-down assay in Arabidopsis thaliana and Oryza sativa proteins
  • dot blot assay of MBP recombinant G protein of Oryza sativa
  • C3b complement component binding assay

Biochem/physiol Actions

Maltose Binding Protein (MBP) mediates uptake of maltose. MBP is a substrate for chaperone secB. Fusion of proteins with MBP tag at the N -terminus improves their solubility.

Disclaimer

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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存储类别

13 - Non Combustible Solids

wgk

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

法规信息

动植物来源生物产品
常规特殊物品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Junxiu Nong et al.
The Journal of cell biology, 220(4) (2021-03-03)
In Wnt/β-catenin signaling, the β-catenin protein level is deliberately controlled by the assembly of the multiprotein β-catenin destruction complex composed of Axin, adenomatous polyposis coli (APC), glycogen synthase kinase 3β (GSK3β), casein kinase 1α (CK1α), and others. Here we provide
Pin-Yao Huang et al.
The Plant journal : for cell and molecular biology, 79(2), 243-255 (2014-05-23)
Pattern-triggered immunity (PTI) is broad spectrum and manipulation of PTI is believed to represent an attractive way to engineer plants with broad-spectrum disease resistance. PTI is activated upon perception of microbe-associated molecular patterns (MAMPs) by pattern-recognition receptors (PRRs). We have
Valerie Hughes et al.
Clinical and vaccine immunology : CVI, 15(12), 1824-1833 (2008-10-11)
Mycobacterium avium subsp. paratuberculosis causes paratuberculosis, a chronic granulomatous enteritis. Detecting animals with paratuberculosis infections is difficult because the currently available tools have low sensitivity and lack specificity; these tools are prone to generating spurious positive test results caused by
A recombinant two-module form of human properdin is an inhibitor of the complement alternative pathway.
Kouser L, et al.
Molecular Immunology, 73(12), 76-87 (2016)
Protein fusion tags for efficient expression and purification of recombinant proteins in the periplasmic space of E. coli.
Malik A.
3 Biotech, 6(1), 44-44 (2016)

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