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TAZ polyclonal antibody   

  • Katalog # : PAB6881
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  • 100 ug
  • EUR € 289
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  • Specification
  • Product Description:
  • Goat polyclonal antibody raised against synthetic peptide of TAZ.
  • Immunogen:
  • A synthetic peptide corresponding to human TAZ.
  • Sequence:
  • C-HLKTQAEQLHNH
  • Host:
  • Goat
  • Theoretical MW (kDa):
  • 33.5, 30.2, 31.7, 28
  • Reactivity:
  • Human
  • Specificity:
  • This antibody is expected to recognize isoforms 1to 4 (NP_000107.1; NP_851828.1; NP_851829.1; NP_851830.1, respectively).
  • Form:
  • Liquid
  • Purification:
  • Antigen affinity purification
  • Concentration:
  • 0.5 mg/mL
  • Quality Control Testing:
  • Antibody Reactive Against Synthetic Peptide.
  • Recommend Usage:
  • ELISA (1:32000)
    Western Blot (0.3-1 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)
  • TAZ polyclonal antibody (Cat # PAB6881) (0.3 ug/mL) staining of human heart 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:
  • 6901
  • Protein Accession#:
  • NP_000107.1;NP_851828.1;NP_851829.1;NP_851830.1
  • Gene Name:
  • TAZ
  • Gene Alias:
  • BTHS,CMD3A,EFE,EFE2,FLJ27390,G4.5,LVNCX,Taz1,XAP-2
  • Gene Description:
  • tafazzin
  • Gene Summary:
  • This gene encodes a protein that is expressed at high levels in cardiac and skeletal muscle. Mutations in this gene have been associated with a number of clinical disorders including Barth syndrome, dilated cardiomyopathy (DCM), hypertrophic DCM, endocardial fibroelastosis, and left ventricular noncompaction (LVNC). Multiple transcript variants encoding different isoforms have been described. A long form and a short form of each of these isoforms is produced; the short form lacks a hydrophobic leader sequence and may exist as a cytoplasmic protein rather than being membrane-bound. Other alternatively spliced transcripts have been described but the full-length nature of all these transcripts is not known. [provided by RefSeq
  • Other Designations:
  • OTTHUMP00000031946,OTTHUMP00000031947,OTTHUMP00000031948,OTTHUMP00000031949,OTTHUMP00000061673
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