SMPD1,ASM Polyclonal antibody

SMPD1,ASM Polyclonal Antibody for WB, IF/ICC, ELISA

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse

Applications

WB, IF/ICC, ELISA

Conjugate

Unconjugated

Cat no : 30197-1-AP

Synonyms

SMPD1, Sphingomyelin phosphodiesterase, EC:3.1.4.12, aSMase, ASM



Tested Applications

Positive WB detected inhuman placenta tissue
Positive IF/ICC detected inNIH/3T3 cells

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:1000-1:4000
Immunofluorescence (IF)/ICCIF/ICC : 1:200-1:800
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

30197-1-AP targets SMPD1,ASM in WB, IF/ICC, ELISA applications and shows reactivity with human, mouse samples.

Tested Reactivity human, mouse
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen SMPD1,ASM fusion protein Ag32479
Full Name sphingomyelin phosphodiesterase 1, acid lysosomal
Calculated Molecular Weight 70 kDa
Observed Molecular Weight68-70 kDa
GenBank Accession NumberBC041164
Gene Symbol SMPD1
Gene ID (NCBI) 6609
Conjugate Unconjugated
Form Liquid
Purification MethodAntigen affinity purification
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

SMPD1(Sphingomyelin phosphodiesterase) is also named as ASM and belongs to the acid sphingomyelinase family. It is an important enzyme in sphingolipid metabolism and plays key roles in apoptosis, immunity, development, and cancer. The deficient activity of this enzyme results in Types A and B Niemann-Pick disease (NPD). This protein has 4 isoforms produced by alternative splicing. SMPD1 can produce a 60 kDa peptide with its signal peptide missing. As a catalytically inactive 75kDa precursor, after signal peptide cleavage, it was processed into smaller non-glycosylated and rapidly degraded 57kDa form in ER-Golgi complex. And 70kDa mature form with major catalytic activity located in lysosomes, which is further processed into 52kDa form (PMID:25853898, PMID:26499107).

Protocols

Product Specific Protocols
WB protocol for SMPD1,ASM antibody 30197-1-APDownload protocol
IF protocol for SMPD1,ASM antibody 30197-1-APDownload protocol
Standard Protocols
Click here to view our Standard Protocols