NSD1 polyclonal antibody (A01)

Catalog # H00064324-A01

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Size:50 uL
Price: USD $ 243.00
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Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
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QC Test

Western Blot detection against Immunogen (37.99 KDa) .

  • Specification

    Product Description

    Mouse polyclonal antibody raised against a partial recombinant NSD1.

    Immunogen

    NSD1 (NP_071900, 2 a.a. ~ 109 a.a) partial recombinant protein with GST tag.

    Sequence

    DQTCELPRRNCLLPFSNPVNLDAPEDKDSPFGNGQSNFSEPLNGCTMQLSTVSGTSQNAYGQDSPSCYIPLRRLQDLASMINVEYLNGSADGSESFQDPEKSDSRAQT

    Host

    Mouse

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (90); Rat (42)

    Quality Control Testing

    Antibody Reactive Against Recombinant Protein.

    Western Blot detection against Immunogen (37.99 KDa) .

    Storage Buffer

    50 % glycerol

    Storage Instruction

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

  • Applications

    Western Blot (Recombinant protein)

    ELISA

  • Gene Info — NSD1

    Entrez GeneID

    64324

    GeneBank Accession#

    NM_022455

    Protein Accession#

    NP_071900

    Gene Name

    NSD1

    Gene Alias

    ARA267, DKFZp666C163, FLJ10684, FLJ22263, FLJ44628, KMT3B, SOTOS, STO

    Gene Description

    nuclear receptor binding SET domain protein 1

    Omim ID

    117550 130650 277590 601626 606681

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes a protein containing a SET domain, 2 LXXLL motifs, 3 nuclear translocation signals (NLSs), 4 plant homeodomain (PHD) finger regions, and a proline-rich region. The encoded protein enhances androgen receptor (AR) transactivation, and this enhancement can be increased further in the presence of other androgen receptor associated coregulators. This protein may act as a nucleus-localized, basic transcriptional factor and also as a bifunctional transcriptional regulator. Mutations of this gene have been associated with Sotos syndrome and Weaver syndrome. One version of childhood acute myeloid leukemia is the result of a cryptic translocation with the breakpoints occurring within nuclear receptor-binding Su-var, enhancer of zeste, and trithorax domain protein 1 on chromosome 5 and nucleoporin, 98-kd on chromosome 11. Two transcript variants encoding distinct isoforms have been identified for this gene. [provided by RefSeq

    Other Designations

    androgen receptor-associated coregulator 267

  • Interactome
  • Pathway
  • 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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