GPD1L Antibody (Clone AT14E2)

GPD1L is converts sn-glycerol 3-phosphate to glycerone phosphate. This protein is found in the cytoplasm, associated with the plasma membrane, where it binds the sodium channel, voltage-gated, type V, alpha subunit (SCN5A). GPD1L is thought to affect trafficking of the cardiac sodium current to the cell surface. Mutations in GPD1L are the cause of sudden infant death syndrome (SIDS) and Brugada syndrome type 2, an autosomal dominant tachyarrhythmia.
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Properties

Data Sheet Click for Datasheet
Catalog Number MA01288
Size 100 µL
Host Type Mouse
Immunogen Recombinant human GPD1L (1-351aa) purified from E. coli
Specificity
Isotype Mouse IgG1, k
Reacitivity Human
Clone Anti-human GPD1L mAb, clone AT14E2, is derived from hybridization of mouse F0 myeloma cells with spleen cells from BALB/c mice immunized with a recombinant human GPD1L protein
Uniprot
Concentration 1mg/ml
Dilution
Formulation Liquid. In Phosphate-Buffered Saline (pH 7.4) with 0.02% Sodium Azide, 10% Glycerol.
Application ELISA, WB, Flow cytometry, ICC/IF
Other Names Glycerol-3-phosphate dehydrogenase 1-like protein, GPD1-L
Storage Lyophilized product: 5 years at 2 - 8°C; Solution: 2 years at -20°C.
Postscript For research use only, not for use in diagnostic procedures.

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