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Serine palmitoyltransferase, which consists of two different subunits, is the key enzyme in sphingolipid biosynthesis. Additionally we are shipping serine Palmitoyltransferase, Long Chain Base Subunit 1 Proteins (9) and serine Palmitoyltransferase, Long Chain Base Subunit 1 Kits (3) and many more products for this protein.
Showing 10 out of 107 products:
Human Polyclonal SPTLC1 Primary Antibody for EIA, WB - ABIN357776
Stachowitz, Alessandrini, Abeck, Ring, Behrendt: Permeability barrier disruption increases the level of serine palmitoyltransferase in human epidermis. in The Journal of investigative dermatology 2002
Show all 5 references for ABIN357776
Human Polyclonal SPTLC1 Primary Antibody for EIA, WB - ABIN357775
Nicholson, Dawkins, Blair, Auer-Grumbach, Brahmbhatt, Hulme: Hereditary sensory neuropathy type I: haplotype analysis shows founders in southern England and Europe. in American journal of human genetics 2001
Show all 5 references for ABIN357775
Human Monoclonal SPTLC1 Primary Antibody for IF, WB - ABIN968462
Hanada, Hara, Nishijima, Kuge, Dickson, Nagiec: A mammalian homolog of the yeast LCB1 encodes a component of serine palmitoyltransferase, the enzyme catalyzing the first step in sphingolipid synthesis. in The Journal of biological chemistry 1998
Show all 2 references for ABIN968462
Human Polyclonal SPTLC1 Primary Antibody for IHC (fro), WB - ABIN4620353
He, Guan, Ong, Farooqui, Wenk: Expression, activity, and role of serine palmitoyltransferase in the rat hippocampus after kainate injury. in Journal of neuroscience research 2007
Human Polyclonal SPTLC1 Primary Antibody for WB - ABIN389109
Wei, Yerokun, Leipelt, Haynes, Radhakrishna, Momin, Kelly, Park, Wang, Carton, Uhlinger, Merrill: Serine palmitoyltransferase subunit 1 is present in the endoplasmic reticulum, nucleus and focal adhesions, and functions in cell morphology. in Biochimica et biophysica acta 2009
Chicken Polyclonal SPTLC1 Primary Antibody for WB - ABIN2782714
Bi, Gao, Yao, Dong, Headley, Yuan: Hereditary sensory and autonomic neuropathy type I in a Chinese family: British C133W mutation exists in the Chinese. in Neuropathology : official journal of the Japanese Society of Neuropathology 2007
Chicken Polyclonal SPTLC1 Primary Antibody for IHC, WB - ABIN2782713
McCampbell, Truong, Broom, Allchorne, Gable, Cutler, Mattson, Woolf, Frosch, Harmon, Dunn, Brown: Mutant SPTLC1 dominantly inhibits serine palmitoyltransferase activity in vivo and confers an age-dependent neuropathy. in Human molecular genetics 2005
The roles of the LCB2a (show SPTLC2 Antibodies) and LCB2b (show SPTLC3 Antibodies) subunits in sphingolipid biosyntesis in A. thaliana were studied.
Hereditary sensory and autonomic neuropathy type 1 mutations in SPTLC1 have distinct biochemical properties, which allowed for the prediction of the clinical symptoms on the basis of the plasma sphingoid base profile.
This study describe aberrant morphology of SPTLC1C133W Dorsal Root Ganglia characterized by increased neurite growth, branching, and expression of p-ERM (show ETV5 Antibodies) at neuronal growth cones.
A novel SPTLC2 (show SPTLC2 Antibodies)-S384F variant in 2 unrelated HSAN1 families resulted in elevated plasma 1-deoxySL levels. Expression of this mutant in HEK293 cells increased 1-deoxySL formation. The substrate specificity is affected by phosphorylation at this position.
Therefore, Ser331 in SPTLC1 is a crucial amino acid, which characterizes the Hereditary sensory and autonomic neuropathy type I phenotype
SPTLC1 mutations cause mitochondrial abnormalities and ER stress in HSN1 cells.
Endoplasmic reticulum-resident human protein serine palmitoyltransferase long chain-1 (SPTLC1) is phosphorylated at Tyr (show TYR Antibodies)(164) by the tyrosine kinase ABL.
The p.CYS133Trp mutation in SPTLC1 is the most common cause of hereditary and autonomic neuropathy in the United Kingdom population.
SPTLC1 mutations p.S331F and p.A352V result in a reduction of serine palmitoyltransferase activity in vitro and are associated with increased levels of the deoxysphingoid in patients' plasma samples.
Hereditary sensory neuropathy type 1 is caused by a gain of function mutation in SPTLC1 which causes the accumulation of two neurotoxic sphingolipids
A novel missense mutation in exon 13 of the SPTLC1 gene (c.1160G-->C; p.G387A) in twin sisters with a severe HSN (show FSCN1 Antibodies) I phenotype is reported.
Data suggest that overexpression of serine palmitoyltransferase (Sptlc1, serine palmitoyltransferase long chain base subunit 1) to elevate de novo sphingolipid biosynthesis induces autophagy in the liver.
Both Sptlc1 and Sptlc2 (show SPTLC2 Antibodies) interactions are necessary for Serine palmitoyl-CoA transferase (SPT (show AGXT Antibodies)) activity in vivo and SPT (show AGXT Antibodies) activity directly influences plasma sphingolipid levels
The expression and activities of SPT (show AGXT Antibodies) in mouse liver increased significantly following fumonisin B1 treatment
Physical interaction of ABCA1 (show ABCA1 Antibodies) and SPTLC1 results in reduction of ABCA1 (show ABCA1 Antibodies) activity and that inhibition of this interaction produces enhanced cholesterol efflux.
Sptlc1 deficient mice absorb less cholesterol.
Serine palmitoyltransferase, which consists of two different subunits, is the key enzyme in sphingolipid biosynthesis. It converts L-serine and palmitoyl-CoA to 3-oxosphinganine with pyridoxal 5'-phosphate as a cofactor. The product of this gene is the long chain base subunit 1 of serine palmitoyltransferase. Mutations in this gene were identified in patients with hereditary sensory neuropathy type 1. Alternatively spliced variants encoding different isoforms have been identified.
Serine palmitoyltransferase 1
, LCB 1
, SPT 1
, long chain base biosynthesis protein 1
, serine C-palmitoyltransferase
, serine palmitoyltransferase 1
, serine-palmitoyl-CoA transferase 1
, serine palmitoyltransferase subunit 1
, Long chain base biosynthesis protein 1
, Serine-palmitoyl-CoA transferase 1
, serine palmitoyltransferase LCB1 subunit