KCNJ2 purified MaxPab mouse polyclonal antibody (B01P)

Catalog # H00003759-B01P

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Size:500 ug
Price: USD $ 1,300.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
  • Specification

    Product Description

    Mouse polyclonal antibody raised against a full-length human KCNJ2 protein.MaxPab Polyclonal Antibody,MaxPab Polyclonal Antibodies,MaxPab,DNA Immune,DNA Immunization,Immune Technology

    Immunogen

    KCNJ2 (NP_000882.1, 1 a.a. ~ 427 a.a) full-length human protein.

    Sequence

    MGSVRTNRYSIVSSEEDGMKLATMAVANGFGNGKSKVHTRQQCRSRFVKKDGHCNVQFINVGEKGQRYLADIFTTCVDIRWRWMLVIFCLAFVLSWLFFGCVFWLIALLHGDLDASKEGKACVSEVNSFTAAFLFSIETQTTIGYGFRCVTDECPIAVFMVVFQSIVGCIIDAFIIGAVMAKMAKPKKRNETLVFSHNAVIAMRDGKLCLMWRVGNLRKSHLVEAHVRAQLLKSRITSEGEYIPLDQIDINVGFDSGIDRIFLVSPITIVHEIDEDSPLYDLSKQDIDNADFEIVVILEGMVEATAMTTQCRSSYLANEILWGHRYEPVLFEEKHYYKVDYSRFHKTYEVPNTPLCSARDLAEKKYILSNANSFCYENEVALTSKEEDDSENGVPESTSTDTPPDIDLHNQASVPLEPRPLRRESEI

    Host

    Mouse

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (98); Rat (99)

    Quality Control Testing

    Antibody reactive against mammalian transfected lysate.

    Storage Buffer

    In 1x PBS, pH 7.4

    Storage Instruction

    Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.

  • Applications

    Western Blot (Transfected lysate)

  • Gene Info — KCNJ2

    Entrez GeneID

    3759

    GeneBank Accession#

    NM_000891.2

    Protein Accession#

    NP_000882.1

    Gene Name

    KCNJ2

    Gene Alias

    HHBIRK1, HHIRK1, IRK1, KIR2.1, LQT7, SQT3

    Gene Description

    potassium inwardly-rectifying channel, subfamily J, member 2

    Omim ID

    170390 600681 609622

    Gene Ontology

    Hyperlink

    Gene Summary

    Potassium channels are present in most mammalian cells, where they participate in a wide range of physiologic responses. The protein encoded by this gene is an integral membrane protein and inward-rectifier type potassium channel. The encoded protein, which has a greater tendency to allow potassium to flow into a cell rather than out of a cell, probably participates in establishing action potential waveform and excitability of neuronal and muscle tissues. Mutations in this gene have been associated with Andersen syndrome, which is characterized by periodic paralysis, cardiac arrhythmias, and dysmorphic features. [provided by RefSeq

    Other Designations

    cardiac inward rectifier potassium channel|inward rectifier K+ channel KIR2.1|inward rectifier potassium channel 2|potassium inwardly-rectifying channel J2

  • Interactome
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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