AK1 (Human) Matched Antibody Pair

Catalog # H00000203-AP15

Size

Price

Stock

Quantity

Size:1 Set
Price: USD $ 607.00
Stock:
order now, ship in 2 weeks
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

Sandwich ELISA detection sensitivity ranging from 1 ng/ml to 100 ng/ml.

  • Specification

    Product Description

    This antibody pair set comes with a matched antibody pair to detect and quantify the protein level of human AK1.

    Reactivity

    Human

    Quality Control Testing

    Standard curve using recombinant protein ( H00000203-P01 ) as an analyte.

    Sandwich ELISA detection sensitivity ranging from 1 ng/ml to 100 ng/ml.

    Supplied Product

    Antibody pair set content:
    1. Capture antibody: rabbit MaxPab® affinity purified polyclonal anti-AK1 (100 ug)
    2. Detection antibody: mouse monoclonal anti-AK1, IgG1 Kappa (20 ug)
    *Reagents are sufficient for at least 1-2 x 96 well plates using recommended protocols.

    Storage Instruction

    Store reagents of the antibody pair set at -20°C or lower. Please aliquot to avoid repeated freeze thaw cycle. Reagents should be returned to -20°C storage immediately after use.

  • Applications

    ELISA Pair (Recombinant protein)

  • Gene Info — AK1

    Entrez GeneID

    203

    Gene Name

    AK1

    Gene Alias

    -

    Gene Description

    adenylate kinase 1

    Omim ID

    103000

    Gene Ontology

    Hyperlink

    Gene Summary

    Adenylate kinase is an enzyme involved in regulating the adenine nucleotide composition within a cell by catalyzing the reversible transfer of phosphate group among adinine nucleotides. Three isozymes of adenylate kinase have been identified in vertebrates, adenylate isozyme 1 (AK1), 2 (AK2) and 3 (AK3). AK1 is found in the cytosol of skeletal muscle, brain and erythrocytes, whereas AK2 and AK3 are found in the mitochondria of other tissues including liver and heart. AK1 was identified because of its association with a rare genetic disorder causing nonspherocytic hemolytic anemia where a mutation in the AK1 gene was found to reduce the catalytic activity of the enzyme. [provided by RefSeq

    Other Designations

    ATP-AMP transphosphorylase|OTTHUMP00000022217|OTTHUMP00000022218|myokinase

  • Interactome
  • Pathway
  • 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