ZRB1714
Anti-p-ATF-2-Thr69/71 Antibody, clone 1H23 ZooMAb® Rabbit Monoclonal

recombinant, expressed in HEK 293 cells
Synonym(s):
Cyclic AMP-dependent transcription factor ATF-2;cAMP-dependent transcription factor ATF-2;Activating transcription factor 2;Cyclic AMP-responsive element-binding protein 2;CREB-2;cAMP-responsive element-binding protein 2;HB16;cAMP response element-binding
About This Item
biological source
rabbit
Quality Level
recombinant
expressed in HEK 293 cells
conjugate
unconjugated
antibody form
purified antibody
antibody product type
primary antibodies
clone
1H23, recombinant monoclonal
description
recombinant, expressed in HEK 293 cells
product line
ZooMAb® learn more
form
lyophilized
mol wt
calculated mol wt 54.54 kDa
observed mol wt ~65 kDa
purified by
using Protein A
species reactivity
human
species reactivity (predicted by homology)
canine, monkey, mouse, rat, porcine
packaging
antibody small pack of 25 μL
greener alternative product characteristics
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enhanced validation
recombinant expression
Learn more about Antibody Enhanced Validation
sustainability
Greener Alternative Product
technique(s)
affinity binding assay: suitable
immunohistochemistry: suitable
inhibition assay: suitable
western blot: suitable
isotype
IgG
epitope sequence
N-terminus
Protein ID accession no.
UniProt accession no.
greener alternative category
shipped in
ambient
Storage temp.
2-8°C
target post-translational modification
phosphorylation (pThr69/pThr71)
Gene Information
human ... ATF2(1386)
General description
Specificity
Immunogen
Application
Evaluated by Western Blotting in lysate from HeLa cells treated with Anisomycin.
Western Blotting Analysis (WB): A 1:10,000 dilution of this antibody detected ATF2 phosphorylated at Threonine 69 and 71 in lysate from HeLa cells, overnight serum starved and treated with Anisomycin (25 g/mL; 30 min), but not in lysate from untreated cells.
Tested applications
Western Blotting Analysis: A 1:10,000 dilution of this antibody detected a construct containing MBP-tagged recombinant fragment of ATF-2 phosphorylated on threonine 69/71, but did not detect in non-phosphorylated construct. (Phospho- ATF-2 construct: Courtesy of Dr. Jesse Rinehart, Yale University, School of Medicine).
Peptide Inhibition Assay Analysis: Target band detection in lysate from HeLa cells treated with Anisomycin was prevented by preblocking of a representative lot with the immunogen phosphopeptide, but not the corresponding non-phosphopeptide.
Affinity Binding Assay: A representative lot of this antibody bound Phospho-ATF-2-Thr69/71 peptide with a KD of 2.1 x 10-8 in an affinity binding assay.
Immunohistochemistry (Paraffin) Analysis: A 1:100 dilution from a representative lot detected Phospho-ATF-2-Thr69/71 in human lung cancer tissue sections.
Note: Actual optimal working dilutions must be determined by end user as specimens, and experimental conditions may vary with the end user
Evaluated by Western Blotting in lysate from HeLa cells treated with Anisomycin.
Western Blotting Analysis (WB): A 1:10,000 dilution of this antibody detected ATF2 phosphorylated at Threonine 69 and 71 in lysate from HeLa cells, overnight serum starved and treated with Anisomycin (25 g/mL; 30 min), but not in lysate from untreated cells.
Target description
Physical form
Reconstitution
Storage and Stability
Legal Information
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Storage Class
11 - Combustible Solids
wgk_germany
WGK 1
flash_point_f
Not applicable
flash_point_c
Not applicable
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