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Rabbit anti-Human CHRND Polyclonal Antibody

The antibody against CHRND was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 22-245 of human CHRND (NP_000742.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

ADA-01551A

The antibody against CHRND was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 22-245 of human CHRND (NP_000742.1) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.

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Specifications


Cat.No ADA-01551A ClonalityPolyclonal
Host SpeciesRabbitTarget NameCHRND
Target SynonymsACHRD; CMS2A; CMS3A; CMS3B; CMS3C; FCCMS; SCCMS; CHRNDFormLiquid
Species ReactivityHuman, MouseIsotypeIgG
Storage Buffer50% Glycerol, PBS with 0.01% thimerosal, pH7.3.Purification MethodAffinity purification
Positive SamplesHeLa, 293T, A-431, Mouse lungApplicationELISA, WB

Immunogen Information


Immunogen DescriptionRecombinant fusion protein containing a sequence corresponding to amino acids 22-245 of human CHRND (NP_000742.1).Target SpeciesHuman
Uniprot IDQ07001Immunogen Sequence
Background Information
  • Uniprot Id

    Q07001

  • Target Species

    Human

  • Target Name

    CHRND

  • Target Full Name

    Acetylcholine receptor subunit delta

  • Target Function

    After binding acetylcholine, the AChR responds by an extensive change in conformation that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane.

  • Target Involvement

    Multiple pterygium syndrome, lethal type (LMPS); Myasthenic syndrome, congenital, 3A, slow-channel (CMS3A); Myasthenic syndrome, congenital, 3B, fast-channel (CMS3B); Myasthenic syndrome, congenital, 3C, associated with acetylcholine receptor deficiency (CMS3C)

  • Target Subcellular Location

    Cell junction, synapse, postsynaptic cell membrane; Multi-pass membrane protein. Cell membrane; Multi-pass membrane protein.

  • Target Protein Families

    Ligand-gated ion channel (TC 1.A.9) family, Acetylcholine receptor (TC 1.A.9.1) subfamily, Delta/CHRND sub-subfamily

  • Target Synonyms

    ACHRD; CMS2A; CMS3A; CMS3B; CMS3C; FCCMS; SCCMS; CHRND

  • Target Background

    The acetylcholine receptor of muscle has 5 subunits of 4 different types: 2 alpha and 1 each of beta, gamma and delta subunits. After acetylcholine binding, the receptor undergoes an extensive conformation change that affects all subunits and leads to opening of an ion-conducting channel across the plasma membrane. Defects in this gene are a cause of multiple pterygium syndrome lethal type (MUPSL), congenital myasthenic syndrome slow-channel type (SCCMS), and congenital myasthenic syndrome fast-channel type (FCCMS). Several transcript variants encoding different isoforms have been found for this gene.

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