Human GPD1L antibody
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.
Product Specifications
Product Name Alternative
Glycerol-3-phosphate dehydrogenase 1-like protein, GPD1-L
Host
Mouse
Antigen Species
Human
Reactivity
Human
Immunogen
Recombinant human GPD1L (1-351aa) purified from E. coli
Clonality
Monoclonal
Isotype
IgG1 κ
Clone
AT14E2
Conjugation
Unconjugated
Applications
ELISA, WB, ICC/IF
Purification Method
By protein-A affinity chromatography
Concentration
1 mg/mL (determined by BCA assay)
Additionnal Information
References & Citations
Valdivia CR., et al. (2009) Am. J. Physiol. 297: H1446-H1452.; ; Van Norstrand DW., et al. (2007) Circulation. 116: 2253-2259.;
Storage Conditions
Can be stored at 2°C to 8°C for 1 week. For long term storage, aliquot and store at -20C to -80C. Avoid repeated freezing and thawing cycles.
Formulation
Liquid in. Phosphate-Buffered Saline (pH 7.4) with 0.02% Sodium Azide, 10% glycerol
Applications Notes
Scientific Category
Signal Transduction
NCBI Accession Number
NP_055956
Uniprot Accession Number
Q8N335
WB Description
IF Description
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