Immunocytochemistry/ Immunofluorescence: BTBD12 Antibody [NBP1-28680] - HeLa cells were fixed for 10 minutes using 10% formalin and then permeabilized for 5 minutes using 1X TBS + 0.5% Triton-X100. The cells were ...read more
Immunohistochemistry-Paraffin: BTBD12 Antibody [NBP1-28680] - IHC analysis of a formalin fixed and paraffin embedded tissue section of human breast infiltrating duct carcinoma using BTBD12 antibody at 1:250 dilution. ...read more
The immunogen recognized by this antibody maps to a region between residue 1784 to 1834 of human SLX4 using the numbering given in entry NP_115820.2 (GeneID 84464).
Isotype
IgG
Clonality
Polyclonal
Host
Rabbit
Gene
SLX4
Purity
Immunogen affinity purified
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Chromatin Immunoprecipitation reported in scientific literature (PMID 24012755)
Immunocytochemistry/ Immunofluorescence 5 - 10 ug/ml. Use reported in scientific literature (PMID 24012755)
Immunohistochemistry 1:250 - 1:500
Immunohistochemistry-Paraffin 1:250 - 1:500
Immunoprecipitation 10 ug/mg lysate
Western Blot reported in scientific literature (PMID 24012755)
Application Notes
Antibody has not performed satisfactorily when used for WB of BTBD12 in crude preparations (e.g. whole cell lysate). This antibody can be used for WB of enriched (e.g. immunoprecipitated) sources of BTBD12. For IHC: Epitope retrieval with citrate buffer pH 6.0 is recommended.
Publications
Read Publications using NBP1-28680 in the following applications:
SLX4 structure-specific endonuclease subunit homolog (S. cerevisiae)
SLX4
Background
BTBD12 (BTBD12 domain-containing protein 12) has been identified as the human ortholog of the yeast Slx4p and drosophila MUS312 DNA repair factors. BTBD12 is an ATM/ATR checkpoint substrate that functions as part of a Holliday junction resolvase and is important for DNA interstrand crosslink repair.
Limitations
This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.
FANCD2 (Fanconi anemia subunit D2 protein) Fanconi anemia (FANC) is a rare, autosomal-recessive genetic disorder that is a heterogeneous cancer susceptibility condition that manifests with a wide range of symptoms such as congenital malformations, deteriorating bone marrow failure, DNA-dama... Read full blog post.
FANCD2: A big component of the DNA repair crew The genetic disorder known as Fanconi anemia (FANC) is a heterogeneous, autosomal-recessive cancer susceptibility condition characterized by a wide array of symptoms. These include congenital malformations, progressive bone marrow failure, DNA-damage ... Read full blog post.
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