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Phospho-CCNE1-pT395 Antibody

Catalog Number:OM217182
OM217182
Discount Price
OM217182-100ul
1~2 Week
100ul
OM217182-50ul
50ul
OM217182-20ul
20ul
1~2 Week
Product Profile
Product Name Phospho-CCNE1-pT395 Antibody
Antibody Type Primary Antibodies
Modification p-T395
Key Feature
Clonality Polyclonal
Isotype Ig
Host Species Rabbit
Tested Applications DBWBIHC
DB:1:500 WB
Species Reactivity Human
Concentration 1mg/ml
Target Information
Gene Synonyms CCNE
Alternative Names CCNE1
CCNE
G1/S-specific cyclin-E1
Molecular Weight(MW) 47077 Da
Function Essential for the control of the cell cycle at the G1/S (start) transition
Tissue Specificity Highly expressed in testis and placenta. Low levels in bronchial epithelial cells
Cellular Localization Nucleus.
Database Links
Entrez Gene 898
Application

Application

Dot blot analysis of anti-Phospho-Cyclin E1-T395 Pab on nitrocellulose membrane. 50ng of Phospho-peptide or Non Phospho-peptide per dot were adsorbed. Antibody working concentrations are 0.5ug per ml.

Application

The anti-Phospho-Cyclin E1-T395 Pab is used in Western blot to detect Phospho-Cyclin E1-T395 in Hela tissue lysate.

Application

Formalin-fixed and paraffin-embedded human cancer tissue reacted with the primary antibody, which was peroxidase-conjugated to the secondary antibody, followed by AEC staining. This data demonstrates the use of this antibody for immunohistochemistry; clinical relevance has not been evaluated. BC = breast carcinoma; HC = hepatocarcinoma.
Application Notes DB:1:500 WB
Additional Information
Form Liquid
Storage Instructions For short-term storage, store at 4° C. For long-term storage, aliquot and store at -20ºC or below. Avoid multiple freeze-thaw cycles.
Storage Buffer Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is first purified by protein G affinity chromatography. Then, the antibody fraction is peptide affinity purified in a 2-step procedure with control and phosphorylated peptides. The phospho-specific antibody is eluted with high and low pH buffers and neutralized immediately, followed by dialysis against PBS.
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