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          • Proteins & Peptides ›
          • CKAP2L Proteins

          Invitrogen

          Human CKAP2L (aa 166-280) Control Fragment Recombinant Protein

          View all (3) CKAP2L proteins

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          Cite Human CKAP2L (aa 166-280) Control Fragment Recombinant Protein

          Product Details

          RP-98213

          Applications
          Tested Dilution
          Publications

          Control (Ctrl)

          Assay-dependent
          -

          Blocking Assay (BLOCK)

          Assay-dependent
          -
          Product Specifications

          Species

          Human

          Expression System

          E. coli

          Amino acid sequence

          MNNIHVENESLDNFLKETNKENLLDILTEPERKPDPKLYTRSKPKTDSYNQTKNSLVPKQALGKSSVNSAVLKDRVNKQFVGETQSRTFPVKSQQLSRGADLARPGVKPSRTVPS

          Tag

          His-ABP-tag

          Class

          Recombinant

          Type

          Protein

          Purity

          >80% by SDS-PAGE and Coomassie blue staining

          Conjugate

          Unconjugated Unconjugated Unconjugated

          Form

          Liquid

          Concentration

          ≥5.0 mg/mL

          Purification

          purified

          Storage buffer

          1M urea/PBS, pH 7.4

          Contains

          no preservative

          Storage conditions

          -20°C, Avoid Freeze/Thaw Cycles

          Product Specific Information

          Highest antigen sequence indentity to the following orthologs: Mouse (51%), Rat (51%).

          This recombinant protein control fragment may be used for blocking experiments with the corresponding antibody, PA5-59048. In IHC/ICC and WB experiments, we recommend a 100x molar excess of the protein fragment control based on the concentration and the molecular weight. Pre-incubate the antibody-protein control fragment mixture for 30 min at room temperature.

          Target Information

          The protein encoded by this gene is thought to be a mitotic spindle protein important to neural stem or progenitor cells. Mutations in this gene have been associated with spindle organization defects, including mitotic spindle defects, lagging chromosomes, and chromatin bridges. There is evidence that mutations in this gene are associated with Filippi syndrome, characterized by growth defects, microcephaly, intellectual disability, facial feature defects, and syndactyly. There is a pseudogene of this gene on chromosome 20. 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: cytoskeleton associated protein 2-like; Cytoskeleton-associated protein 2-like; FLJ40629; Radial fiber and mitotic spindle protein; Radmis

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          Gene Aliases: CKAP2L

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          UniProt ID: (Human) Q53RS8

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          Entrez Gene ID: (Human) 150468

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          It has to be done as per old AB suggested Products section.
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