OPLAH Antibody
Product Specifications
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.
Product Datasheet
https://www.prosci-inc.com/?datasheet_sku=14-232
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
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