Bio-Connect
WB analysis of 293 cell lysate in (A) the absence and (B) the presence of blocking peptide using GTX32055 B9D1 antibody. Working concentration : 1 microg/ml
WB analysis of 293 cell lysate in (A) the absence and (B) the presence of blocking peptide using GTX32055 B9D1 antibody. Working concentration : 1 microg/ml
WB analysis of 293 cell lysate in (A) the absence and (B) the presence of blocking peptide using GTX32055 B9D1 antibody. Working concentration : 1 microg/ml

B9D1 antibody

GTX32055
GeneTex
ApplicationsImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry
Product group Antibodies
ReactivityHuman
TargetB9D1
Sign in to order and to see your custom pricing.
Large volume orders?
Order with a bulk request

Overview

  • Supplier
    GeneTex
  • Product Name
    B9D1 antibody
  • Delivery Days Customer
    9
  • Antibody Specificity
    At least two isoforms of B9D1 are known to exist; this antibody will only recognize the longest isoform. B9D1 antibody is predicted to not cross-react with other DNAJC family members.
  • Application Supplier Note
    WB: 1 microg/mL. ICC/IF: 5 microg/mL. *Optimal dilutions/concentrations should be determined by the researcher.Not tested in other applications.
  • Applications
    ImmunoFluorescence, Western Blot, ELISA, ImmunoCytoChemistry
  • Certification
    Research Use Only
  • Clonality
    Polyclonal
  • Concentration
    1 mg/ml
  • Conjugate
    Unconjugated
  • Gene ID27077
  • Target name
    B9D1
  • Target description
    B9 domain containing 1
  • Target synonyms
    B9; B9 domain-containing protein 1; B9 protein domain 1; endothelial precursor protein B9; EPPB9; JBTS27; MKS1-related protein 1; MKS9; MKSR1; MKSR-1
  • Host
    Rabbit
  • Isotype
    IgG
  • Protein IDQ9UPM9
  • Protein Name
    B9 domain-containing protein 1
  • Scientific Description
    This gene encodes a B9 domain-containing protein, one of several that are involved in ciliogenesis. Alterations in expression of this gene have been found in a family with Meckel syndrome. Meckel syndrome has been associated with at least six different genes. This gene is located within the Smith-Magenis syndrome region on chromosome 17. Three alternatively spliced transcript variants that encode different proteins have been described for this gene. [provided by RefSeq, Aug 2011]
  • Reactivity
    Human
  • Storage Instruction
    -20°C or -80°C,2°C to 8°C
  • UNSPSC
    12352203