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Invitrogen™ GPD1L Polyclonal Antibody

Rabbit Polyclonal Antibody
Supplier: Invitrogen™ PA5114389
Description
Reconstitute with 0.2 mL of distilled water to yield a concentration of 500 μg/mL. Positive Control - WB: human placenta issue, human PC-3 whole cell, human U-87MG whole cell, human HL-60 whole cell, human HepG2 whole cell, human A549 whole cell, human Caco-2 whole cell, human K562 whole cell, rat heart issue, mouse RAW2467 whole cell. Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month. It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.
The protein encoded by this gene catalyzes the conversion of sn-glycerol 3-phosphate to glycerone phosphate. The encoded protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). Defects in this gene are a cause of Brugada syndrome type 2 (BRS2) as well as sudden infant death syndrome (SIDS).
Specifications
GPD1L | |
Polyclonal | |
Unconjugated | |
GPD1L | |
2210409H23Rik; D9Ertd660e; glycerol-3-phosphate dehydrogenase 1-like; glycerol-3-phosphate dehydrogenase 1-like protein; Gpd1l; GPD1-L; Kiaa0089; RGD1560123 | |
Rabbit | |
Affinity chromatography | |
RUO | |
23171, 333433, 363159 | |
-20°C | |
Lyophilized |
ELISA, Western Blot | |
500 μg/mL | |
PBS with 4mg trehalose and 0.05mg sodium azide | |
Q3ULJ0, Q8N335 | |
GPD1L | |
E.coli-derived human GPD1L recombinant protein (Position: A19-T351). | |
100 μg | |
Primary | |
Human, Mouse, Rat | |
Antibody | |
IgG |
Safety and Handling
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