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AK2 Rabbit mAb

     
  • 1 - AK2 Rabbit mAb AP76382
    Immunocytochemistry analysis of AK2 (green) in Hela using AK2 antibody,and DAPI(blue).
  • 2 - AK2 Rabbit mAb AP76382
    Western blot analysis of AK2 in Hela, CHO-K1, C6, mouse Brain, Ramos lysates using AK2 antibody.
  • 8 - AK2 Rabbit mAb AP76382
    Immunohistochemistry analysis of paraffin-embedded Human tonsil using AK2 antibody. High-pressure and temperature Sodium Citrate pH 6.0 was used for antigen retrieval.
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Product Information
Application
  • Applications Legend:
  • E=ELISA
  • WB=Western Blotting
  • IHC=Immunohistochemistry
  • IHC-P=Immunohistochemistry (Paraffin)
  • IP=Immunoprecipitation
  • IF=Immunofluorescence
  • IC=Immunochemistry
  • ICC=Immunocytochemistry
  • FC=Flow Cytometry
  • DB=Dot Blot
WB, IHC-P, IHC-F, IP
Primary Accession P54819
Reactivity Rat, Human, Mouse
Host Rabbit
Clonality Monoclonal Antibody
Isotype IgG
Conjugate Unconjugated
Purification Affinity Purified
Calculated MW 26478 Da
Additional Information
Gene ID 204
Other Names AK2
Dilution WB~~1:1000-1:5000
IHC-P~~1:50~200
IHC-F~~N/A
IP~~1:10-1:100
Format Liquid in 50mM Tris-Glycine(pH 7.4), 0.15M NaCl, 40%Glycerol, 0.01% sodium azide and 0.05% BSA.
StorageStore at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.
Protein Information
Name AK2 {ECO:0000255|HAMAP-Rule:MF_03168}
Synonyms ADK2
Function Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP. Plays an important role in cellular energy homeostasis and in adenine nucleotide metabolism. Adenylate kinase activity is critical for regulation of the phosphate utilization and the AMP de novo biosynthesis pathways. Plays a key role in hematopoiesis.
Cellular Location Mitochondrion intermembrane space {ECO:0000255|HAMAP-Rule:MF_03168}
Tissue Location Present in most tissues. Present at high level in heart, liver and kidney, and at low level in brain, skeletal muscle and skin. Present in thrombocytes but not in erythrocytes, which lack mitochondria. Present in all nucleated cell populations from blood, while AK1 is mostly absent. In spleen and lymph nodes, mononuclear cells lack AK1, whereas AK2 is readily detectable. These results indicate that leukocytes may be susceptible to defects caused by the lack of AK2, as they do not express AK1 in sufficient amounts to compensate for the AK2 functional deficits (at protein level)
Research Areas

For Research Use Only. Not For Use In Diagnostic Procedures.

BACKGROUND

Catalyzes the reversible transfer of the terminal phosphate group between ATP and AMP.

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