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MABE1068

Sigma-Aldrich

Anti-APE/Ref-1 Antibody, clone 13B8E5C2

clone 13B8E5C2, from mouse

Synonyme(s) :

DNA-(apurinic or apyrimidinic site) lyase, AP endonuclease 1, APE-1, APEN, APEX nuclease, Apurinic-apyrimidinic endonuclease 1, Redox factor-1, REF-1

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100 μG
502,00 $

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100 μG
502,00 $

About This Item

Code UNSPSC :
12352203
eCl@ss :
32160702

502,00 $


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Devis pour commande en gros

Source biologique

mouse

Niveau de qualité

Forme d'anticorps

purified antibody

Type de produit anticorps

primary antibodies

Clone

13B8E5C2, monoclonal

Espèces réactives

human, rat, mouse

Technique(s)

immunocytochemistry: suitable
immunohistochemistry: suitable (paraffin)
western blot: suitable

Isotype

IgG2aκ

Numéro d'accès NCBI

Numéro d'accès UniProt

Conditions d'expédition

ambient

Modification post-traductionnelle de la cible

unmodified

Informations sur le gène

human ... HAP1(9001)

Description générale

DNA-(apurinic or apyrimidinic site) lyase (EC 4.2.99.18; UniProt P27695; also known as AP endonuclease 1, APE-1, APEN, APEX nuclease, Apurinic-apyrimidinic endonuclease 1, Redox factor-1, REF-1) is encoded by the APEX1 (also known as APE, APE1, APEX, APX, HAP1, REF1) gene (Gene ID 328) in human. APE/Ref-1 mediates the cleavage of an apurinic/apyrimidinic (AP) site in DNA generated by DNA glycosylases during base excision repair (BER) in both nucleus and mitochondria. APE/Ref-1 also functions as a redox factor (ref) responsible for maintaining several transcription factors (TFs) in an active reduced state for DNA binding, including AP-1, NF-κB, HIF-1α, CREB, TP53. Elevated levels of APE1 are associated with resistance to chemotherapyand poor prognosis in various cancers. APE/Ref-1 is synthesized as a 318-a.a. protein whose initiation methionine (Met1) is removed posttranslationally to yield the 317-a.a. form with a nuclear localization sequence (NLS; a.a. 8-13) and a nuclear export signal (NES; a.a. 64-80) sequence to allow its shuttle between the cytoplasm and nucleus. The 317-a.a. form can be further processed by a mitochondria-associated N-terminal peptidase into a mitochrondrial form (mtAPE; a.a. 32-318) that lacks NLS and contains only the NES and the mitochondrial targeting sequence (MTS; a.a. 289-318).

Spécificité

Clone 13B8E5C2 detected both cytosolic and nuclear APE/Ref-1 by Immunocytochemistry, Immunohistochemistry, and Western blotting (Moore, D.H., et al. (2000). Clin. Cancer Res. 6(2):602-609).

Immunogène

Recombinant full-length human APE/Ref-1.

Application

Anti-APE/Ref-1, clone 13B8E5C2, Cat. No. MABE1068, is a highly specific mouse monoclonal antibody, that targets APE1 and has been tested in Immunocytochemistry, Immunohistochemistry (Paraffin), and Western Blotting.
Immunocytochemistry Analysis: A 1:200 dilution from a representative lot detected both cytosolic and nuclear APE/Ref-1 immunoreactivity in 4% paraformaldehyde-fixed, 0.3% Triton X-100-permeabilized HeLa cells.

Immunohistochemistry Analysis: A 1:1,000 dilution from a representative lot detected nuclear APE/Ref-1 immunoreactivity in rat kidney, and human placenta & small intestine tissue sections.

Western Blotting Analysis: 0.5 µg/mL from a representative lot detected APE/Ref-1 in 10 µg of Raji cell lysate.

Immunocytochemistry Analysis: A representative lot detected both cytosolic and nuclear APE/Ref-1 immunoreactivity in HeyC2 and HEY human ovarian cancer cell lines (Moore, D.H., et al. (2000). Clin. Cancer Res. 6(2):602-609).

Immunohistochemistry Analysis: A representative lot detected varying tissue distribution and cellular localization of APE/Ref-1 immunoreactivity among various 4% formaldehyde-fixed, paraffin-embedded human ovarian tissue samples, including ovarian endometriosis, serous cystadenoma , serous carcinoma, ands well as normal ovarian tissues (Moore, D.H., et al. (2000). Clin. Cancer Res. 6(2):602-609).

Western Blotting Analysis: A representative lot detected an upregulated cytosolic APE/Ref-1 level in HeyC2 than HEY cells, while similar nuclear APE/Ref-1 level was detected in these two human ovarian cancer cell lines (Moore, D.H., et al. (2000). Clin. Cancer Res. 6(2):602-609).

Qualité

Evaluated by Western Blotting in HepG2 cell lysate.

Western Blotting Analysis: 0.5 µg/mL of this antibody detected APE/Ref-1 in 10 µg of HepG2 cell lysate.

Description de la cible

~35-39 kDa observed. 35.42 kDa (Met1 removed; a.a. 2-318) and 32.24 kDa (Mitochondrial form; a.a. 32-318) calculated. The broad banding pattern is consistent with the detection of both mitochondrial and non-mitochondrial forms with varying degrees of posttranslational modifications (lysine acetylation, threonine phosphorylation, cysteine nitrosylation). Uncharacterized bands may be observed in some lysate(s).

Forme physique

Format: Purified

Autres remarques

Concentration: Please refer to lot specific datasheet.

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Code de la classe de stockage

12 - Non Combustible Liquids

Classe de danger pour l'eau (WGK)

WGK 1


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