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Phospho-Akt-T308 Rabbit mAb (AP1259)

Review (1)Publications (11) Datasheet

Tested applications:WBIHC-PIF/ICCIPChIPChIP-seqRIPFCFC(Intra)ELISAMeDIPNucleotide ArrayDBFACSCoIPCUT&TagmeRIPInhibitionReactivity:Mouse, Rat

ABclonal:Western blot - Phospho-Akt-T308 Rabbit mAb (AP1259)

Western blot analysis of various lysates using Phospho-Akt-T308 Rabbit mAb (AP1259) at 1:1000 dilution. NIH/3T3 and C6 cells were treated by Calyculin A (100 nM) at 37℃ for 30 minutes after serum-starvation overnight.
Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
Lysates/proteins: 25μg per lane.
Blocking buffer: 3% nonfat dry milk in TBST.
Detection: ECL Basic Kit (RM00020).
Exposure time: 180s.

Review
ABclonal: review for Phospho-Akt-T308 Rabbit mAb(AP1259)

Overview

Product namePhospho-Akt-T308 Rabbit mAb
Catalog No.AP1259
Host speciesRabbit
Purification methodAffinity purification
IsotypeIgG
CloneNo.ARC50457
The serine-threonine protein kinase encoded by the AKT1 gene is catalytically inactive in serum-starved primary and immortalized fibroblasts. AKT1 and the related AKT2 are activated by platelet-derived growth factor. The activation is rapid and specific, and it is abrogated by mutations in the pleckstrin homology domain of AKT1. It was shown that the activation occurs through phosphatidylinositol 3-kinase. In the developing nervous system AKT is a critical mediator of growth factor-induced neuronal survival. Survival factors can suppress apoptosis in a transcription-independent manner by activating the serine/threonine kinase AKT1, which then phosphorylates and inactivates components of the apoptotic machinery. Mutations in this gene have been associated with the Proteus syndrome. Multiple alternatively spliced transcript variants have been found for this gene.
ImmunogenA synthetic phosphorylated peptide around T308 of human Akt (NP_005154.2).
SequenceMKTFC
Gene ID
Swiss Prot
SynonymsAKT1/AKT2/AKT3; Phospho-Akt-T308
Calculated MW48kDa/55kDa/51kDa/54kDa
Observed MW60kDa
ReactivityMouse, Rat
Tested applicationsWBIHC-PIF/ICCIPChIPChIP-seqRIPFCFC(Intra)ELISAMeDIPNucleotide ArrayDBFACSCoIPCUT&TagmeRIPInhibition
Recommended dilution
  • WB 1:500 - 1:1000
Storage bufferStore at -20℃. Avoid freeze / thaw cycles.
Buffer: PBS with 0.05% proclin300, 0.05% BSA, 50% glycerol, pH7.3.
Key applicationWestern blotting    
Positive samplesNIH/3T3 treated by Calyculin A, C6 treated by Calyculin A
Cellular locationCiliary basal body, Cytoplasm, Cytosol, Microtubule cytoskeleton, Mitochondrion, Nucleoplasm, Nucleus, Plasma membrane, Spindle.
Customer validation

(14 um cryosections from 7 dpf zebrafish larvae)

WB(Mus musculus, Homo sapiens, Rattus norvegicus, Other)

IF(Rattus norvegicus)

Documents

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    ABclonal:Western blot - Phospho-Akt-T308 Rabbit mAb (AP1259)}

    Western blot - Phospho-Akt-T308 Rabbit mAb (AP1259)

    Western blot analysis of various lysates using Phospho-Akt-T308 Rabbit mAb (AP1259) at 1:1000 dilution. NIH/3T3 and C6 cells were treated by Calyculin A (100 nM) at 37℃ for 30 minutes after serum-starvation overnight.
    Secondary antibody: HRP-conjugated Goat anti-Rabbit IgG (H+L) (AS014) at 1:10000 dilution.
    Lysates/proteins: 25μg per lane.
    Blocking buffer: 3% nonfat dry milk in TBST.
    Detection: ECL Basic Kit (RM00020).
    Exposure time: 180s.

    * For research use only. Not for therapeutic or diagnostic purposes.

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    Secondary Antibodies (26)