HR polyclonal antibody (A01)

Catalog # H00055806-A01

Size

Price

Stock

Quantity

Size:50 uL
Price: USD $ 243.00
Stock:
order now, ship next day
abnova-minus
abnova-plus

* The price is valid only in USA. Please select country.

Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
Images
QC Test

Western Blot detection against Immunogen (37.11 KDa) .

  • Specification

    Product Description

    Mouse polyclonal antibody raised against a partial recombinant HR.

    Immunogen

    HR (NP_005135, 1090 a.a. ~ 1189 a.a) partial recombinant protein with GST tag.

    Sequence

    LDAGLRRRLREEWGVSCWTLLQAPGEAVLVPAGAPHQVQGLVSTVSVTQHFLSPETSALSAQLCHQGPSLPPDCHLLYAQMDWAVFQAVKVAVGTLQEAK

    Host

    Mouse

    Reactivity

    Human

    Interspecies Antigen Sequence

    Mouse (91)

    Quality Control Testing

    Antibody Reactive Against Recombinant Protein.

    Western Blot detection against Immunogen (37.11 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 — HR

    Entrez GeneID

    55806

    GeneBank Accession#

    NM_005144

    Protein Accession#

    NP_005135

    Gene Name

    HR

    Gene Alias

    ALUNC, AU, HSA277165

    Gene Description

    hairless homolog (mouse)

    Omim ID

    203655 209500 602302

    Gene Ontology

    Hyperlink

    Gene Summary

    This gene encodes a protein that is involved in hair growth. This protein functions as a transcriptional corepressor of multiple nuclear receptors, including thyroid hormone receptor, the retinoic acid receptor-related orphan receptors and the vitamin D receptors, and it interacts with histone deacetylases. The translation of this protein is modulated by multiple regulatory ORFs that exist upstream of the primary ORF. Mutations in one of these upstream ORFs, U2HR, cause Marie Unna hereditary hypotrichosis (MUHH), an autosomal dominant form of genetic hair loss. Mutations in this gene also cause autosomal recessive congenital alopecia and atrichia with papular lesions, other diseases resulting in hair loss. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq

    Other Designations

    OTTHUMP00000122609|OTTHUMP00000159164|hairless protein

  • Interactome
  • Disease
Contact Info
  • +1-909-264-1399
    +1-909-992-0619
    Toll Free : +1-877-853-6098
  • +1-909-992-3401
4 Products to Compare
Remove All