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  2. Polyclonal

GTX02580

PLCE1 antibody

Cannot supply to this region.

SKU:
GTX02580
Additional Names:
phospholipase C epsilon 1 , NPHS3 , PLCE , PPLC
Application:
WB, IHC-P, IF, ICC
Concentration:
1 mg/ml
Physical State:
Liquid
Species Reactivity:
Human
Purification:
Affinity Purified
Storage Conditions:
-20[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., 2-8[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted., -20[o]C/-70[o]C Aliquot. Avoid freeze/thaw cycles. Store undiluted.
Supplier:
Genetex
Host:
Rabbit
Reactivities:
Human, Mouse, Rat
Buffer:
PBS, 150mM NaCl, 50% Glycerol, 0.02% Sodium azide.
Immunogen:
A synthesized peptide derived from human PLCE1, corresponding to a region within C-terminal amino acids.
Uniprot:
Q9P212
Synonyms:
1-phosphatidylinositol 4,5-bisphosphate phosphodiesterase epsilon-1;NPHS3;pancreas-enriched phospholipase C;phosphoinositide phospholipase C;phosphoinositide phospholipase C-epsilon-1;phosphoinositide-specific phospholipase C epsilon-1;Phospholipase C-epsilon-1;PLC-epsilon-1;PLCE;PPLC
Extra Details:
This gene encodes a phospholipase enzyme that catalyzes the hydrolysis of phosphatidylinositol-4,5-bisphosphate to generate two second messengers: inositol 1,4,5-triphosphate (IP3) and diacylglycerol (DAG). These second messengers subsequently regulate various processes affecting cell growth, differentiation, and gene expression. This enzyme is regulated by small monomeric GTPases of the Ras and Rho families and by heterotrimeric G proteins. In addition to its phospholipase C catalytic activity, this enzyme has an N-terminal domain with guanine nucleotide exchange (GEF) activity. Mutations in this gene cause early-onset nephrotic syndrome; characterized by proteinuria, edema, and diffuse mesangial sclerosis or focal and segmental glomerulosclerosis. Alternative splicing results in multiple transcript variants encoding distinct isoforms.[provided by RefSeq, Sep 2009]
Shipping Conditions:
Blue Ice