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Rabbit anti-Human RCN2 Polyclonal Antibody

The antibody against RCN2 was raised in rabbit using the Recombinant Human Reticulocalbin-2 protein (23-180AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.

ADC-16826A

The antibody against RCN2 was raised in rabbit using the Recombinant Human Reticulocalbin-2 protein (23-180AA) as the immunogen. This antibody exists as a non-conjugated isotype IgG, Antigen affinity purified. This antibody has been validated on ELISA, IHC.

$299.00

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Specifications


Cat.No ADC-16826A ClonalityPolyclonal
Host SpeciesRabbitTarget NameRCN2
FormLiquidSpecies ReactivityHuman
IsotypeIgGStorage Buffer50% Glycerol, PBS with 0.02% sodium azide, pH7.3.
Purification MethodAntigen affinity purifiedConjugateNon-conjugated
ApplicationELISA, IHCStorageUpon receipt

Immunogen Information


Immunogen DescriptionRecombinant Human Reticulocalbin-2 protein (23-180AA)Target SpeciesHuman
Immunogen SequenceComplete sequences for the immunogen, target protein, and peptides are available upon request.Uniprot IDQ14257
Background Information
  • Uniprot Id

    Q14257

  • Target Species

    Human

  • Target Name

    RCN2

  • Target Full Name

    Reticulocalbin-2

  • Target Function

    Not known. Binds calcium.

  • Target Subcellular Location

    Endoplasmic reticulum lumen.

  • Target Protein Families

    CREC family

  • Target Tissue Specificity

    Ubiquitous.

  • Target Synonyms

    Calcium binding protein ERC 55 ; Calcium-binding protein ERC-55; E6 binding protein; E6-binding protein; E6BP; ERC 55 ; ERC55 ; Rcn2; RCN2_HUMAN; Reticulocalbin 2 EF hand calcium binding domain (endoplasmic reticulum calcium binding protein 55kD); Reticulocalbin 2; EF hand calcium binding domain ; Reticulocalbin-2; TCBP49

  • Target Background

    The protein encoded by this gene is a calcium-binding protein located in the lumen of the ER. The protein contains six conserved regions with similarity to a high affinity Ca(+2)-binding motif, the EF-hand. This gene maps to the same region as type 4 Bardet-Biedl syndrome, suggesting a possible causative role for this gene in the disorder. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.

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