SPTLC1 Recombinant monoclonal antibody

SPTLC1 Uni-rAb® Recombinant Antibody for WB, ELISA
Cat No. 87141-1-RR
Clone No.252268G2

Host / Isotype

Rabbit / IgG

Reactivity

human

Applications

WB, ELISA

EC:2.3.1.50, HSAN1, LCB 1, LCB1, Serine-palmitoyl-CoA transferase 1

Formulation:  PBS, Azide, Glycerol
PBS, Azide, Glycerol
PBS Only
Conjugate:  Unconjugated
Unconjugated
Size/Concentration: 

-/ -

Freight/Packing: -

Quantity

Please visit your regions distributor:


Tested Applications

Positive WB detected inHeLa cells, HepG2 cells, Jurkat cells, HEK-293 cells

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:5000-1:50000
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Product Information

87141-1-RR targets SPTLC1 in WB, ELISA applications and shows reactivity with human samples.

Tested Reactivity human
Host / Isotype Rabbit / IgG
Class Recombinant
Type Antibody
Immunogen

CatNo: Ag1162

Product name: Recombinant human SPTLC1 protein

Source: e coli.-derived, PGEX-4T

Tag: GST

Domain: 1-143 aa of BC007085

Sequence: MATATEQWVLVEMVQALYEAPAYHLILEGILILWIIRLLFSKTYKLQERSDLTVKEKEELIEEWQPEPLVPPVPKDHPALNYNIVSGPPSHKTVVNGKECINFASFNFLGLLDNPRVKAAALASLKKYGVGTCGPRGFYGTFE

Predict reactive species
Full Name serine palmitoyltransferase, long chain base subunit 1
Calculated Molecular Weight 53 kDa
Observed Molecular Weight53 kDa
GenBank Accession NumberBC007085
Gene Symbol SPTLC1
Gene ID (NCBI) 10558
Conjugate Unconjugated
FormLiquid
Purification MethodProtein A purification
UNIPROT IDO15269
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol, pH 7.3.
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA.

Background Information

SPTLC1 is a subunit of serine palmitoyltransferase (SPT) which is the key enzyme in sphingolipid biosynthesis and is essential for embryogenesis and cell survival. Mutations in the SPTLC1 gene (C133W, C133Y, V144D, and G387A) were reported to be responsible for the development of an inherited sensory neuropathy (hereditary sensory neuropathy type I, HSN1) (PMID: 39959268). Pathogenic variants in SPTLC1 are causative for hereditary sensory and autonomic neuropathy, juvenile amyotrophic lateral sclerosis, macular telangiectasia type 2, or Charcot-Marie-Tooth disease (PMID: 31751474). Western blot analysis detected a specific band at ~53 kDa (PMID: 36197001).

Protocols

Product Specific Protocols
WB protocol for SPTLC1 antibody 87141-1-RRDownload protocol
Standard Protocols
Click here to view our Standard Protocols
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