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Anti-Maltose Binding Protein antibody [R29.6]
Anti-Maltose Binding Protein antibody [R29.6] from Abcam
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Citations:
(5)
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Supplier Page from
Abcam for
Anti-Maltose Binding Protein antibody [R29.6]
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Product Specs
Item
Anti-Maltose Binding Protein antibody [R29.6]
Company
Abcam
Price
Supplier Page
View Company Product Page
Catalog Number
ab65
Host
Mouse
Isotype
IgG1
Clone
R29.6
Quantity
50 µg
Clonality
Monoclonal
Applications
ChIP, IP, WB
Conjugate/Tag
Unconjugated
Concentration
1.8 mg/ml
Gene Name
malE
Reactivity
Escherichia coli
NCBI Gene Aliases
HUX90_07730
Antibody Type
Primary Antibody
Target
malE
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Questions and Answers
Can this antibody be used for ChIP assays, and if so, how has it been utilized in research?
Yes, the Anti-Maltose Binding Protein antibody has been shown to work in Chromatin Immunoprecipitation (ChIP) assays. For instance, in a study by Liu et al. (2006), the antibody was employed to perform ChIP, allowing researchers to investigate the binding locations of the yeast transcription factor Leu3 in vivo.
What specific bacterial species does this antibody react with, and how might that be relevant for my experiments?
This antibody is reactive with Escherichia species. This specificity is particularly relevant for experiments involving maltose binding protein fusion proteins in bacterial systems, allowing for targeted studies in bacterial cell biology and protein interactions.
Is this antibody suitable for use in Western blotting, and what kind of results can I expect?
The Anti-Maltose Binding Protein antibody is suitable for Western blotting applications. While specific results may vary depending on the experimental conditions, it has been cited in multiple studies, indicating its effectiveness in detecting maltose binding protein fusion proteins in various experimental setups.
What is the host species for this antibody, and does that affect its performance in different applications?
The host species for this antibody is mouse, and it is classified as a monoclonal IgG1 isotype. The choice of host species can influence the antibody's performance in applications such as immunoprecipitation and Western blotting, as mouse-derived antibodies typically exhibit strong specificity and affinity for their target antigens.
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Abcam
Discovery Drive
Cambridge Biomedical Campus
Cambridge
CB2 0AX
United Kingdom
Phone
: +44 (0) 1223 696000 (option 1)
+44 (0) 1223 696000 (option 2)
+44 (0) 1223 771600
Company Profile
Website:
http://www.abcam.com
Citations (5)
(1)
Characterization of Cyanate Metabolism in Marine
Synechococcus
and
Prochlorococcus
spp
Applied and Environmental Microbiology
January 1, 2011
Nina A. Kamennaya, Anton F. Post
three times with TBS buffer containing 0.01% Tween 20 (TTBS). Primary antibody (MBP antibody [R29.6];
ab65
;
Abcam
) diluted
1:1,000
was added, followed by
incubation
overnight at 4°C, and then washed with TTBS
(2)
Differential Bacterial Surface Display of Peptides by the Transmembrane Domain of OmpA
PLoS ONE
August 25, 2009
Gertjan S. Verhoeven, Svetlana Alexeeva, Marileen Dogterom, Tanneke den den Blaauwen
antibody was used in a
1:10000
dilution (upper blot) and the monoclonal anti-
MBP
antibody (
Abcam
, #
ab65
) was used at a concentration of 1.8 mg/ml (lower blot). Found at: doi:10.1371/journal.pone.0006739.
s006
(3)
Structure and function of the ESCRT-II-III interface in multivesicular body biogenesis
Developmental cell
August 1, 2009
Young Jun Im, Thomas Wollert, Evzen Boura, James H Hurley
(4)
Whole-genome comparison of Leu3 binding in vitro and in vivo reveals the importance of nucleosome occupancy in target site selection
Genome Research
December 1, 2006
Xiao Liu, Cheol-Koo Lee, Joshua A. Granek, Neil D. Clarke, Jason D. Lieb
Schimmel 1995; Wang et al. 1999). ChIP was performed as described (Lieb et al. 2001) with anti-MBP (
Abcam
ab65
) and
protein G agarose
(
Sigma
83,219), except that following the IP, the
protein G agarose
was washed
(5)
DIP-chip: Rapid and accurate determination of DNA-binding specificity
Genome Research
March 1, 2005
Xiao Liu, David M. Noll, Jason D. Lieb, Neil D. Clarke
average size of ∼0.5 kb. We carried out ChIP
assays
as described (Lieb et al. 2001) with anti-MBP (
Abcam
ab65
) and
protein G agarose
(
SIGMA
83219), except that after the ChIP, we washed protein G-agarose beads
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Anti-Maltose Binding Protein antibody [R29.6] from Abcam
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