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Last updated: 2016/12/4
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DLX5 polyclonal antibody

  • Catalog # : PAB13670
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  • Specification
  • Product Description:
  • Goat polyclonal antibody raised against synthetic peptide of DLX5.
  • Immunogen:
  • A synthetic peptide corresponding to amino acids at internal region of human DLX5.
  • Sequence:
  • C-AYNRVPSATNQPEK
  • Host:
  • Goat
  • Theoretical MW (kDa):
  • 31.5
  • Reactivity:
  • Human
  • Specificity:
  • Approximately 30 KDa band observed in human bone marrow lysates (calculated MW of 31.5 KDa according to NP_005212.1). The observed molecular weight corresponds to earlier findings in literature with different antibodies (Lee et al, J Biol Chem. 2003 Sep 5;278(36):34387-94; PMID: 12815054).
  • Form:
  • Liquid
  • Purification:
  • Antigen affinity purification
  • Concentration:
  • 0.5 mg/mL
  • Recommend Usage:
  • ELISA (1:32000)
    Western Blot (1-3 ug/mL)
    The optimal working dilution should be determined by the end user.
  • Storage Buffer:
  • In Tris saline, pH 7.3 (0.5% BSA, 0.02% sodium azide)
  • 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.
  • Publication Reference
  • Applications
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • DLX5 polyclonal antibody (Cat # PAB13670) (1 ug/mL) staining of human bone marrow lysate (35 ug protein in RIPA buffer). Primary incubation was 1 hour. Detected by chemiluminescence.
  • ELISA
  • Application Image
  • Western Blot (Tissue lysate)
  • Western Blot (Tissue lysate)
  • enlarge
  • ELISA
  • Gene Information
  • Entrez GeneID:
  • 1749
  • Gene Name:
  • DLX5
  • Gene Alias:
  • -
  • Gene Description:
  • distal-less homeobox 5
  • Gene Summary:
  • This gene encodes a member of a homeobox transcription factor gene family similiar to the Drosophila distal-less gene. The encoded protein may play a role in bone development and fracture healing. Mutation in this gene, which is located in a tail-to-tail configuration with another member of the family on the long arm of chromosome 7, may be associated with split-hand/split-foot malformation. [provided by RefSeq
  • Other Designations:
  • distal-less homeo box 5
  • Related Disease
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