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MAB8121 Anti-Cytomegalovirus Antibody, blend, clone 8B1.2, 1G5.2, and 2D4.2

MAB8121
100 µg  
Purchase on Sigma-Aldrich

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Overview

Replacement Information

Key Spec Table

Species ReactivityKey ApplicationsHostFormatAntibody Type
HIF, IHCMPurifiedMonoclonal Antibody
Description
Catalogue NumberMAB8121
Brand Family Chemicon®
Trade Name
  • Chemicon
DescriptionAnti-Cytomegalovirus Antibody, blend, clone 8B1.2, 1G5.2, and 2D4.2
Alternate Names
  • CMV
References
Product Information
FormatPurified
Presentation0.02 M PB, 0.25M NaCl, PH 7.6 with 0.1% Sodium Azide.
Quality LevelMQ300
Applications
ApplicationThis Anti-Cytomegalovirus Antibody, blend, clone 8B1.2, 1G5.2 & 2D4.2 is validated for use in IF, IH for the detection of Cytomegalovirus.
Key Applications
  • Immunofluorescence
  • Immunohistochemistry
Application NotesImmunohistochemistry

Immunofluorescence

Optimal working dilutions must be determined by the end user.
Biological Information
ImmunogenMRC-5 infected cells with ATCC VR538 and AD169, ultrasonicated, screened by plate reduction neutralization tests.
Epitopeblend
Clone8B1.2, 1G5.2, and 2D4.2
HostMouse
SpecificityReacts with Immediate early, early, and late antigen preparations. Can detect CMV infection within 2 hours post-infection exhibiting a nuclear staining which reaches peak intensity between 48 and 96 hours. This antigen is persisting and can be detected during the complete CMV infection cycle. Staining of CMV structural antigens becomes apparent at about 48 hours. Extra-nuclear staining is first seen in the region of the golgi apparatus followed subsequently by staining of viral proteins and particles in the cytoplasm.

With CMV the antigens expressed at different times are listed as:



Immediate Early (alpha gene expression): those antigens expressed at 3-12 hrs post-infection generally involved in Transcription such as 72kD major phosphoprotein and a few other other antigens at 60 - 80kD.

Early Antigen (beta genes) a.k.a. Delayed Early or Intermediate Early: expressed at 12-24hrs post-infection. Generally enzymes and one virion structural gene preceding viral DNA synthesis.

Late Antigen (gamma genes): expressed at 36-48hrs post-infection. Generally structural proteins. Major protein = 55kD
IsotypeIgG2a
Species Reactivity
  • Human
Antibody TypeMonoclonal Antibody
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Usage Statement
  • 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.
Storage and Shipping Information
Storage ConditionsMaintain at +2-8C in convenient aliquots for up to 6 months. Do not freeze.
Packaging Information
Material Size100 µg
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
Catalogue Number GTIN
MAB8121 04053252612206

Documentation

Anti-Cytomegalovirus Antibody, blend, clone 8B1.2, 1G5.2, and 2D4.2 SDS

Title

Safety Data Sheet (SDS) 

Anti-Cytomegalovirus Antibody, blend, clone 8B1.2, 1G5.2, and 2D4.2 Certificates of Analysis

TitleLot Number
MOUSE ANTI-CYTOMEGALOVIRUS (Blend) MONOCLONAL ANTIBODY - 2344687 2344687
MOUSE ANTI-CYTOMEGALOVIRUS (Blend) MONOCLONAL ANTIBODY - 2153032 2153032
MOUSE ANTI-CYTOMEGALOVIRUS (Blend) - 2489031 2489031
MOUSE ANTI-CYTOMEGALOVIRUS (Blend) - 3069692 3069692
MOUSE ANTI-CYTOMEGALOVIRUS (Blend) - 3451415 3451415
MOUSE ANTI-CYTOMEGALOVIRUS (Blend) - 3484051 3484051
MOUSE ANTI-CYTOMEGALOVIRUS (Blend) - 3695880 3695880
MOUSE ANTI-CYTOMEGALOVIRUS (Blend) - 3845341 3845341
MOUSE ANTI-CYTOMEGALOVIRUS (Blend) - 4034300 4034300
MOUSE ANTI-CYTOMEGALOVIRUS (Blend) - 4082579 4082579

References

Reference overviewPub Med ID
Intrauterine growth restriction caused by underlying congenital cytomegalovirus infection.
Pereira, L; Petitt, M; Fong, A; Tsuge, M; Tabata, T; Fang-Hoover, J; Maidji, E; Zydek, M; Zhou, Y; Inoue, N; Loghavi, S; Pepkowitz, S; Kauvar, LM; Ogunyemi, D
The Journal of infectious diseases  209  1573-84  2014

Show Abstract
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