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CMPK1 Polyclonal Antibody

SKU: E-AB-52550-200

  • $ 55995


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CMPK1 Polyclonal Antibody

 

SKU # E-AB-52550
Reactivity Human, Mouse, Rat
Host Rabbit
Applications WB 

 

Product Details

Isotype IgG
Host Rabbit
Reactivity Human, Mouse, Rat
Applications WB
Clonality Polyclonal
Immunogen Full length fusion protein
Abbre CMPK1
Synonyms CMK,  CMPK,  CMPK 1,  Cytidine monophosphate (UMP CMP) kinase 1 cytosolic,  Cytidine monophosphate UMP CMP kinase 1 cytosolic,  Cytidine monophosphate kinase,  Cytidylate kinase,  Deoxycytidylate kinase,  EC 2.7.4.14,  KCY,  Monophosphatase kinase,  OTTHU,  cmpk1,  dCMP kinase
Swissprot
Calculated MW 22 kDa
Observed MW Refer to figures
Cellular Localization Nucleus. Cytoplasm. Mainly nuclear.
Concentration 0.66 mg/mL
Buffer Phosphate buffered solution, pH 7.4, containing 0.05% stabilizer and 50% glycerol.
Purification Method Antigen affinity purification
Research Areas Epigenetics and Nuclear Signaling,  Metabolism
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.

 

Related Reagents

Applications Recommended Dilution
WB  1:500-1:2000

 

Background

The product of this gene belongs to the CLC chloride channel family of proteins. Chloride channels play important roles in the plasma membrane and in intracellular organelles. This gene encodes chloride channel 7. Defects in this gene are the cause of osteopetrosis autosomal recessive type 4 (OPTB4), also called infantile malignant osteopetrosis type 2 as well as the cause of autosomal dominant osteopetrosis type 2 (OPTA2), also called autosomal dominant Albers-Schonberg disease or marble disease autosoml dominant. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. OPTA2 is the most common form of osteopetrosis, occurring in adolescence or adulthood.