• All
  • Primary Antibodies
  • Conjugated Antibodies for IF
  • Conjugated Antibodies for FC
  • Secondary Antibodies
  • Antibody Labeling KitsNew
  • ELISA Kits
  • IHC Kits
  • Magnetic Cell Separation Kits
  • Cytokines & Growth Factors
  • Neutralizing/activating Antibodies
  • Nanobody-based Reagents
  • Accessory Products and Kits
  • Fusion Proteins
×
×
Host
0
Species Reactivity
0
Species Reactivity
0
Conjugate
0
Conjugate
0
Compatible Species
0
Conjugate
0
×

Target

Host

Species Reactivity

Species Reactivity

Conjugate

Conjugate

XRCC5 Monoclonal antibody, PBS Only

XRCC5 Monoclonal Antibody for WB, IP, IF, IHC, Indirect ELISA

Host / Isotype

Mouse / IgG1

Reactivity

Human, mouse, rat

Applications

WB, IP, IF, IHC, Indirect ELISA

Conjugate

Unconjugated

CloneNo.

2G5E7

Cat no : 66546-1-PBS

Synonyms

86 kDa subunit of Ku antigen, CTC85, CTCBF, DNA repair protein XRCC5, G22P2, KARP 1, KARP1, KU80, Ku86, KUB2, NFIV, Nuclear factor IV, Thyroid lupus autoantigen, TLAA, XRCC5

Validation Data Gallery

Applications:
  • WB analysis using 66546-1-Ig (same clone as 66546-1-PBS)

    WB analysis using 66546-1-Ig (same clone as 66546-1-PBS)

    Various lysates were subjected to SDS PAGE followed by western blot with 66546-1-Ig (XRCC5 antibody) at dilution of 1:20000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 66546-1-PBS in a different storage buffer formulation.

  • IP experiment of HeLa using 66546-1-Ig (same clone as 66546-1-PBS)

    IP experiment of HeLa using 66546-1-Ig (same clone as 66546-1-PBS)

    IP result of anti-XRCC5 (IP:66546-1-Ig, 5ug; Detection:66546-1-Ig 1:20000) with HeLa cells lysate 3200 ug. This data was developed using the same antibody clone with 66546-1-PBS in a different storage buffer formulation.

  • IP experiment of HeLa using 66546-1-Ig (same clone as 66546-1-PBS)

    IP experiment of HeLa using 66546-1-Ig (same clone as 66546-1-PBS)

    IP result of anti-XRCC5 (IP:66546-1-Ig, 5ug; Detection:66546-1-Ig 1:40000) with HeLa cells lysate 640 ug. This data was developed using the same antibody clone with 66546-1-PBS in a different storage buffer formulation.

  • IHC staining of human lung cancer using 66546-1-Ig (same clone as 66546-1-PBS)

    IHC staining of human lung cancer using 66546-1-Ig (same clone as 66546-1-PBS)

    Immunohistochemical analysis of paraffin-embedded human lung cancer tissue slide using 66546-1-Ig (XRCC5 antibody) at dilution of 1:1000 (under 40x lens. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 66546-1-PBS in a different storage buffer formulation.

    Ready-to-use IHC kits available with XRCC5 antibody included
  • IHC staining of human breast cancer using 66546-1-Ig (same clone as 66546-1-PBS)

    IHC staining of human breast cancer using 66546-1-Ig (same clone as 66546-1-PBS)

    Immunohistochemical analysis of paraffin-embedded human breast cancer tissue slide using 66546-1-Ig (XRCC5 antibody) at dilution of 1:1000 (under 10x lens. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 66546-1-PBS in a different storage buffer formulation.

    Ready-to-use IHC kits available with XRCC5 antibody included
  • IHC staining of human breast cancer using 66546-1-Ig (same clone as 66546-1-PBS)

    IHC staining of human breast cancer using 66546-1-Ig (same clone as 66546-1-PBS)

    Immunohistochemical analysis of paraffin-embedded human breast cancer tissue slide using 66546-1-Ig (XRCC5 antibody) at dilution of 1:1000 (under 10x lens. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 66546-1-PBS in a different storage buffer formulation.

    Ready-to-use IHC kits available with XRCC5 antibody included
  • IHC staining of human lung cancer using 66546-1-Ig (same clone as 66546-1-PBS)

    IHC staining of human lung cancer using 66546-1-Ig (same clone as 66546-1-PBS)

    Immunohistochemical analysis of paraffin-embedded human lung cancer tissue slide using 66546-1-Ig (XRCC5 antibody) at dilution of 1:1000 (under 10x lens. Heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0). This data was developed using the same antibody clone with 66546-1-PBS in a different storage buffer formulation.

    Ready-to-use IHC kits available with XRCC5 antibody included
  • IF Staining of HeLa using 66546-1-Ig (same clone as 66546-1-PBS)

    IF Staining of HeLa using 66546-1-Ig (same clone as 66546-1-PBS)

    Immunofluorescent analysis of (4% PFA) fixed HeLa cells using 66546-1-Ig (XRCC5 antibody) at dilution of 1:100 and Alexa Fluor 488-conjugated AffiniPure Goat Anti-Mouse IgG(H+L). This data was developed using the same antibody clone with 66546-1-PBS in a different storage buffer formulation.

Tested Applications

Planning an IHC experiment? We recommend our IHCeasy XRCC5 Ready-To-Use IHC Kit. XRCC5 primary antibody included.

Recommended dilution

ApplicationDilution
Sample-dependent, check data in validation data gallery

Product Information

66546-1-PBS targets XRCC5 in WB, IP, IF, IHC, Indirect ELISA applications and shows reactivity with Human, mouse, rat samples.

Tested Reactivity Human, mouse, rat
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Immunogen XRCC5 fusion protein Ag9512 相同性解析による交差性が予測される生物種
Full Name X-ray repair complementing defective repair in Chinese hamster cells 5 (double-strand-break rejoining)
Calculated molecular weight 732 aa, 83 kDa
Observed molecular weight 80-83 kDa
GenBank accession numberBC019027
Gene symbol XRCC5
Gene ID (NCBI) 7520
Conjugate Unconjugated
Form Liquid
Purification Method Protein G purification
Storage Buffer PBS Only
Storage ConditionsStore at -80°C.

Background Information

There are at least two pathways for eukaryotes to repair DNA double-strand breaks: homologous recombination and nonhomologous end joining(NHEJ). The core NHEJ machinery includes XRCC4, DNA ligase IV and the DNA-dependent protein kinase complex, which consists of the DNA end-binding XRCC5/XRCC6 heterodimer and the catalytic subunit PRKDC. The heterdimer of XRCC5/XRCC6 enhanced teh affinity of the catalytic subunit PRKDC to DNA by 100-fold. Once the XRCC5/6 dimer association with NAA15, it can bind to the osteocalcin promoter and activate osteocalcin expression. The XRCC5/6 dimer acts as a negative regulator of transcription when together with APEX1. Some publised papers indicated that the MW of XRCC5 is 86kDa, while more papers suggested that XRCC5 is a 80kDa protein, as it was firstly introducted in publication. Thus, Ku80 and Ku86 are the same protein.