GPD1 Antibody
Product Specifications
Background
GPD1L belongs to the NAD-dependent glycerol-3-phosphate dehydrogenase family. Defects in GPD1L are the cause of Brugada syndrome type 2 (BRS2) and sudden infant death syndrome (SIDS) .
NCBI Gene ID
2819
Swiss Prot
P21695
Accession Number
NP_005267
Host
Rabbit
Reactivity
Human
Immunogen
Antibody produced in rabbits immunized with a synthetic peptide corresponding a region of human GPD1.
Clonality
Polyclonal
Conjugation
Unconjugated
Type
Primary Antibodies
Field of Research
Cancer
Purification
Antibody is purified by peptide affinity chromatography method.
Positive Control
Tranfected 293T Cell Lysate
Concentration
Batch dependent
Buffer
Purified antibody supplied in 1x PBS buffer with 0.09% (w/v) sodium azide and 2% sucrose.
Modification
None
Shipping Conditions
Blue Ice
Storage Conditions
For short periods of storage (days) store at 4˚ C. For longer periods of storage, store GPD1 antibody at -20˚ C. As with any antibody avoid repeat freeze-thaw cycles.
Calculated Molecular Weight
37 kDa
Applications Notes
GPD1 antibody can be used for detection of GPD1 by ELISA at 1:62500. GPD1 antibody can be used for detection of GPD1 by western blot at 1 μ g/mL, and HRP conjugated secondary antibody should be diluted 1:50,000 - 100,000.
Symbol
GPD1
NCBI Official Name
Glycerol-3-phosphate dehydrogenase 1 (soluble)
NCBI Organism
Homo sapiens
Background Reference 01
Park, J.J., (2006) Physiol. Genomics 27 (2), 114-121.
Other Product Names
GPD1, FLJ26652, GPD-C, HTGTI, GPDH-C
Tested Applications
ELISA, WB
Protein ID
33695088
Physical Properties
Liquid
Curated Selection
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