Product nameAnti-MTA2/PID antibody
See all MTA2/PID primary antibodies
DescriptionRabbit polyclonal to MTA2/PID
SpecificityNo cross-reactivity to MTA1.
Tested applicationsSuitable for: WB, IHC-Fr, IHC-P, ICC/IF, ELISA, IPmore details
Species reactivityReacts with: Mouse, Rat, Human
- HeLa cell lysate
This product was previously labelled as MTA2
Storage instructionsShipped at 4°C. Store at +4°C.
Storage bufferPreservative: 0.02% Sodium azide
Concentration information loading...
Our Abpromise guarantee covers the use of ab8106 in the following tested applications.
The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.
|WB||Use a concentration of 0.5 - 1 µg/ml. Detects a band of approximately 75 kDa (predicted molecular weight: 75 kDa).|
|IHC-Fr||Use at an assay dependent concentration. PubMed: 18413351|
|IHC-P||Use at an assay dependent concentration.|
|ICC/IF||Use a concentration of 10 µg/ml.|
|ELISA||Use at an assay dependent concentration.|
|IP||Use a concentration of 5 µg/ml.|
FunctionMay be involved in the regulation of gene expression as repressor and activator. The repression might be related to covalent modification of histone proteins.
Tissue specificityWidely expressed.
Sequence similaritiesContains 1 BAH domain.
Contains 1 ELM2 domain.
Contains 1 GATA-type zinc finger.
Contains 1 SANT domain.
- Information by UniProt
- DKFZp686F2281 antibody
- Mata1l1 antibody
- Metastasis associated 1 family member 2 antibody
All lanes : Anti-MTA2/PID antibody (ab8106) at 1 µg/ml
Lane 1 : HeLa whole cell lysate with absence of blocking peptide
Lane 2 : HeLa whole cell lysate with presence of blocking peptide
Predicted band size: 75 kDa
ab8106 at 10µg/ml staining MTA2/PID in Hela cells by ICC/IF
ab8106 (2µg/ml) staining MTA2/PID in human ileum using an automated system (DAKO Autostainer Plus). Using this protocol there is strong nuclear staining.
Sections were rehydrated and antigen retrieved with the Dako 3 in 1 AR buffer EDTA pH 9.0 in a DAKO PT Link. Slides were peroxidase blocked in 3% H2O2 in methanol for 10 mins. They were then blocked with Dako Protein block for 10 minutes (containing casein 0.25% in PBS) then incubated with primary antibody for 20 min and detected with Dako Envision Flex amplification kit for 30 minutes. Colorimetric detection was completed with Diaminobenzidine for 5 minutes. Slides were counterstained with Haematoxylin and coverslipped under DePeX. Please note that, for manual staining, optimization of primary antibody concentration and incubation time is recommended. Signal amplification may be required.
MTA2/PID was immunoprecipitated using 0.5mg Hela whole cell extract, 5µg of Rabbit polyclonal to MTA2/PID and 50µl of protein G magnetic beads (+). No antibody was added to the control (-).
The antibody was incubated under agitation with Protein G beads for 10min, Hela whole cell extract lysate diluted in RIPA buffer was added to each sample and incubated for a further 10min under agitation.
Proteins were eluted by addition of 40µl SDS loading buffer and incubated for 10min at 70oC; 10µl of each sample was separated on a SDS PAGE gel, transferred to a nitrocellulose membrane, blocked with 5% BSA and probed with ab8106.
Secondary: Mouse monoclonal [SB62a] Secondary Antibody to Rabbit IgG light chain (HRP) (ab99697).
Band: 77kDa: MTA2/PID
Immunofluorescence of PID in HeLa cells using ab8106 at 10 ug/ml.
This product has been referenced in:
- Campbell AE et al. NuRD and CAF-1-mediated silencing of the D4Z4 array is modulated by DUX4-induced MBD3L proteins. Elife 7:N/A (2018). Read more (PubMed: 29533181) »
- Christov CP et al. A NuRD Complex from Xenopus laevis Eggs Is Essential for DNA Replication during Early Embryogenesis. Cell Rep 22:2265-2278 (2018). Read more (PubMed: 29490265) »