NIPBL polyclonal antibody

Catalog # PAB18614

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Size:100 ug
Price: USD $ 428.00
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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

    Goat polyclonal antibody raised against synthetic peptide of NIPBL.

    Immunogen

    A synthetic peptide corresponding to amino acids 889-902 at internal region of human NIPBL.

    Sequence

    C-RPDSPRVKQGDSNK

    Host

    Goat

    Specificity

    This antibody is expected to recognize both reported isoforms (NP_597677.2; NP_056199.2).

    Form

    Liquid

    Purification

    Antigen affinity purification

    Concentration

    0.5 mg/mL

    Recommend Usage

    ELISA (1:32000)
    The optimal working dilution should be determined by the end user.

    Storage Buffer

    In 0.5 mg/mL Tris saline, pH 7.3 (0.02% sodium azide, 0.5% BSA)

    Storage Instruction

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

    Note

    This product contains sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

  • Applications

    Enzyme-linked Immunoabsorbent Assay

  • Gene Info — NIPBL

    Entrez GeneID

    25836

    Protein Accession#

    NP_597677.2;NP_056199.2

    Gene Name

    NIPBL

    Gene Alias

    CDLS, CDLS1, DKFZp434L1319, FLJ11203, FLJ12597, FLJ13354, FLJ13648, FLJ44854, IDN3, IDN3-B

    Gene Description

    Nipped-B homolog (Drosophila)

    Omim ID

    122470 608667

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes the homolog of the Drosophila melanogaster Nipped-B gene product and fungal Scc2-type sister chromatid cohesion proteins. The Drosophila protein facilitates enhancer-promoter communication of remote enhancers and plays a role in developmental regulation. It is also homologous to a family of chromosomal adherins with broad roles in sister chromatid cohesion, chromosome condensation, and DNA repair. The human protein has a bipartite nuclear targeting sequence and a putative HEAT repeat. Condensins, cohesins and other complexes with chromosome-related functions also contain HEAT repeats. Mutations in this gene result in Cornelia de Lange syndrome, a disorder characterized by dysmorphic facial features, growth delay, limb reduction defects, and mental retardation. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq

    Other Designations

    OTTHUMP00000116005|SCC2 homolog|delangin|nipped-B-like

  • 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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