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          • Primary Antibodies ›
          • FANCM Antibodies

          Bioss

          FANCM Polyclonal Antibody

          View all (10) FANCM antibodies

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          Cite FANCM Polyclonal Antibody

          Additional Information:
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          FANCM Polyclonal Antibody

          Product Details

          BS-13143R

          Applications
          Tested Dilution
          Publications

          Immunohistochemistry (Paraffin) (IHC (P))

          1:200-1:400
          -

          Immunohistochemistry (Frozen) (IHC (F))

          1:100-1:500
          -

          Immunocytochemistry (ICC/IF)

          1:100-1:500
          -

          ELISA (ELISA)

          1:500-1:1,000
          -
          Product Specifications

          Species Reactivity

          Human

          Host/Isotype

          Rabbit / IgG

          Class

          Polyclonal

          Type

          Antibody

          Immunogen

          KLH conjugated synthetic peptide derived from human FANCM, amino acids 831-930.
          View immunogen

          Conjugate

          Unconjugated Unconjugated Unconjugated

          Form

          Liquid

          Concentration

          1 mg/mL

          Purification

          Protein A

          Storage buffer

          0.01M TBS, pH 7.4, with 1% BSA, 50% glycerol

          Contains

          0.02% ProClin 300

          Storage conditions

          -20°C

          Shipping conditions

          Ambient (domestic); Wet ice (international)

          Target Information

          The Fanconi anemia complementation group (FANC) currently includes FANCA, FANCB, FANCC, FANCD1 (also called BRCA2), FANCD2, FANCE, FANCF, FANCG, FANCI, FANCJ (also called BRIP1), FANCL, FANCM and FANCN (also called PALB2). The previously defined group FANCH is the same as FANCA. Fanconi anemia is a genetically heterogeneous recessive disorder characterized by cytogenetic instability, hypersensitivity to DNA crosslinking agents, increased chromosomal breakage, and defective DNA repair. The members of the Fanconi anemia complementation group do not share sequence similarity; they are related by their assembly into a common nuclear protein complex. This gene encodes the protein for complementation group M. Alternative splicing results in multiple transcript variants.

          For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.

          References (0)

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          Cite this product

          Bioinformatics

          Protein Aliases: ATP-dependent RNA helicase FANCM; FAAP250; FANCM; Fanconi anemia complementation group M; Fanconi anemia group M protein; Fanconi anemia-associated polypeptide of 250 kDa; Protein FACM; Protein Hef ortholog; unnamed protein product

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          Gene Aliases: FAAP250; FANCM; KIAA1596; POF15; SPGF28

          View more View less

          UniProt ID: (Human) Q8IYD8

          View more View less

          Entrez Gene ID: (Human) 57697

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          Function(s)
          nucleotide binding four-way junction DNA binding nucleic acid binding DNA binding chromatin binding RNA helicase activity helicase activity nuclease activity protein binding ATP binding four-way junction helicase activity hydrolase activity ATPase activity 3'-5' DNA helicase activity
          Process(es)
          resolution of meiotic recombination intermediates DNA repair cellular response to DNA damage stimulus replication fork processing reciprocal DNA recombination interstrand cross-link repair double-strand break repair via synthesis-dependent strand annealing positive regulation of protein monoubiquitination
          It has to be done as per old AB suggested Products section.

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