OPLAH Antibody

• Background:

  The protein encoded by this gene acts as a homodimer, using ATP hydrolysis to catalyze the conversion of 5-oxo-L-proline to L-glutamate. Defects in this gene are a cause of 5-oxoprolinase deficiency (OPLAHD) .

• NCBI Gene ID:

  26873

• Swiss Prot:

  O14841

• Host:

  Rabbit

• Reactivity:

  Human, Mouse, Rat

• Immunogen:

  Recombinant fusion protein containing a sequence corresponding to amino acids 1119-1288 of human OPLAH (NP_060040.1) .

• Clonality:

  Polyclonal

• Conjugation:

  Unconjugated

• Type:

  Primary Antibodies

• Field of Research:

  Signal Transduction

• Purification:

  Affinity purification

• Positive Control:

  K-562

• Concentration:

  Batch dependent

• Buffer:

  PBS with 0.02% sodium azide, 50% glycerol, pH7.3.

• Modification:

  None

• Shipping Conditions:

  Blue Ice

• Storage Conditions:

  Store at -20˚ C. Avoid freeze / thaw cycles.

• Calculated Molecular Weight:

  Observed: 134kDa

• Fragment:

  IgG

• Applications Notes:

  WB: 1:500 - 1:2000

• Symbol:

  OPLAH

• Positive Control 2:

  Mouse brain

• Positive Control 3:

  Mouse kidney

• Positive Control 4:

  Mouse liver

• NCBI Official Name:

  5-oxoprolinase, ATP-hydrolysing

• NCBI Organism:

  Homo sapiens

• Other Product Names:

  5-Opase, OPLAD, OPLAH, 5-oxoprolinase, 5-oxo-L-prolinase, pyroglutamase

• Tested Applications:

  WB

• Physical Properties:

  Liquid