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DCLRE1C Antibody (N-term)Peptide Affinity Purified Rabbit Polyclonal Antibody (Pab)

Country
United States
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Ordering Information
Catalog # Size Availability Price  
AP9737a 0.1 mg 400 ul In Stock $ 255.00 Add to cart
AP9737a-ev20 20 ug 100 ul In Stock $ 95.00 Add to cart
  • Specification
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DCLRE1C Antibody (N-term) - Product info

ApplicationWB, IHC
  • Applications Legend:
  • W=Western Blotting
  • IP=Immunoprecipitation
  • IHC-P=Immunohistochemistry (Paraffin)
  • IF-IC=Immunofluorescence (Immunocytochemistry)
  • F=Flow Cytometry
Primary AccessionQ96SD1
ReactivityHuman, Mouse
Concentration0.25 mg/ml
IsotypeRabbit Ig
Calculated MW78436 Da

DCLRE1C Antibody (N-term) - Additional info

Gene ID 64421
Other Names
DCLRE1C; ARTEMIS; ASCID; SCIDA; SNM1C; Protein artemis; DNA cross-link repair 1C protein; Protein A-SCID; SNM1 homolog C; SNM1-like protein
Target/Specificity
This DCLRE1C antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 28~58 amino acids from the N-terminal region of human DCLRE1C.
Dilution
WB~~1:100~500
IHC~~1:50~100
Format
Purified polyclonal antibody supplied in PBS with 0.09% (W/V) sodium azide. This antibody is purified through a protein A column, followed by peptide affinity purification.
Storage
Maintain refrigerated at 2-8°C for up to 6 months. For long term storage store at -20°C in small aliquots to prevent freeze-thaw cycles.
Precautions
DCLRE1C Antibody (N-term) is for research use only and not for use in diagnostic or therapeutic procedures.

DCLRE1C Antibody (N-term) - Protein Information

Name DCLRE1C
Synonyms ARTEMIS, ASCID, SCIDA, SNM1C
Function
Required for V(D)J recombination, the process by which exons encoding the antigen-binding domains of immunoglobulins and T-cell receptor proteins are assembled from individual V, (D), and J gene segments. V(D)J recombination is initiated by the lymphoid specific RAG endonuclease complex, which generates site specific DNA double strand breaks (DSBs). These DSBs present two types of DNA end structures: hairpin sealed coding ends and phosphorylated blunt signal ends. These ends are independently repaired by the non homologous end joining (NHEJ) pathway to form coding and signal joints respectively. This protein exhibits single-strand specific 5'-3' exonuclease activity in isolation and acquires endonucleolytic activity on 5' and 3' hairpins and overhangs when in a complex with PRKDC. The latter activity is required specifically for the resolution of closed hairpins prior to the formation of the coding joint. May also be required for the repair of complex DSBs induced by ionizing radiation, which require substantial end-processing prior to religation by NHEJ
Cellular Location
Nucleus.
Tissue Location
Ubiquitously expressed, with highest levels in the kidney, lung, pancreas and placenta (at the mRNA level) Expression is not increased in thymus or bone marrow, sites of V(D)J recombination

DCLRE1C Antibody (N-term) - Related products

AP9737a: DCLRE1C Antibody (N-term)

BP9737a: DCLRE1C Antibody (N-term) Blocking Peptide

DCLRE1C Antibody (N-term) - Application data

  • Western blot analysis of DCLRE1C Antibody (N-term) (Cat. #AP9737a) in mouse heart tissue lysates (35ug/lane). DCLRE1C (arrow) was detected using the purified Pab.

  • DCLRE1C Antibody (N-term) (Cat. #AP9737a) immunohistochemistry analysis in formalin fixed and paraffin embedded human lung carcinoma followed by peroxidase conjugation of the secondary antibody and DAB staining. This data demonstrates the use of the DCLRE1C Antibody (N-term) for immunohistochemistry. Clinical relevance has not been evaluated.

DCLRE1C Antibody (N-term) - Research Areas

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BACKGROUND

DCLRE1C is a nuclear protein that is involved in V(D)J recombination and DNA repair. The protein has single-strand-specific 5'-3' exonuclease activity; it also exhibits endonuclease activity on 5' and 3' overhangs and hairpins when complexed with protein kinase, DNA-activated, catalytic polypeptide.

REFERENCES

Beucher, A., et al. EMBO J. 28(21):3413-3427(2009) Rivera-Munoz, P., et al. Blood 114(17):3601-3609(2009) Wang, H., et al. J. Biol. Chem. 284(27):18236-18243(2009)