Toll-free:1-888-852-8623

All categories

  • All categories
  • Flow Cytometry Antibodies
  • ELISA Kits
  • MACS Cell Isolation
  • Antibodies and Reagents
  • Cell Health Detection
  • Metabolism Assays
  • Immunoassays
  • Cell Identification
  • Proteins and Peptides
  • Cell Culture
Please enter the item number/product keyword!
Keyword cannot be empty !
INSERT SYMBOLS:
  • α
  • β
  • γ
  • δ
  • ε
  • ζ
  • η
  • θ
  • κ
  • μ
  • ω
  • σ
  • τ
  • λ
  • ⅩⅢ
  • ⅩⅢ
  • ⅩⅣ
  • ⅩⅤ
  • ⅩⅦ
  • ⅩⅧ
  • UP ↑
All Size Price Qty
200μL $ 399.00
120μL $ 240.00
60μL $ 143.00
20μL $ 73.00
Add to cart

For research use only.

Verified Samples Verified Samples in WB: Mouse heart, Human hepatocellsular carcinoma
Verified Samples in IHC: Human breast cancer, Human thyroid cancer
Dilution WB 1:500-1:2000,  IHC 1:50-1:200
Isotype IgG
Host Rabbit
Reactivity Human,  Mouse
Applications WB,  IHC
Clonality Polyclonal
Immunogen Recombinant protein of human HINT2
Abbre HINT2
Synonyms 1190005L05Rik,  HINT-2,  HINT-3,  HINT2,  HIT-17,  HIT-17kDa,  Histidine triad nucleotide-binding protein 2,  PKCI-1-related HIT protein,  Protein kinase C inhibitor 2,  histidine triad nucleotide binding protein 2,  mitochondrial
Swissprot
Calculated MW 17 kDa
Cellular Localization Mitochondrion.
Concentration 0.8 mg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
Purification Method Affinity purification
Research Areas Signal Transduction
Conjugation Unconjugated
Storage Store at -20°C Valid for 12 months. Avoid freeze / thaw cycles.
Shipping The product is shipped with ice pack,upon receipt,store it immediately at the temperature recommended.
background Hint2 (histidine triad nucleotide binding protein 2), also known as HIT-17, is a 163 amino acid secreted protein that contains one HIT domain, a histidine triad that has catalytic activity toward the -phosphate of ribonucleotides.Via its HIT domain, Hint2 is thought to function as a hydrolase that is encoded by a gene whicHuman, Mouseaps to chromosome 9.Chromosome 9 contains 145 million base pairs and comprises 4% of the human genome, encoding nearly 900 genes.Hereditary hemorrhagic telangiectasia and Familial dysautonomia are both associated with chromosome 9.Notably, chromosome 9 encompasses the largest interferon family gene cluster.
Other Clones

{{antibodyDetailsPage.numTotal}} Results

Other Formats

{{formatDetailsPage.numTotal}} Results

Unconjugated

  • IF:{{item.impact}}

    Journal:{{item.journal}} ({{item.year}})

    DOI:{{item.doi}}

    Reactivity:{{item.species}}

    Sample Type:{{item.organization}}

  • Q{{(FAQpage.currentPage - 1)*pageSize+index+1}}:{{item.name}}