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The antibody against SMS was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-366 of human SMS (NP_004586.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.
The antibody against SMS was raised in Rabbit using the recombinant fusion protein containing a sequence corresponding to amino acids 1-366 of human SMS (NP_004586.2) as the immunogen. The polyclonal antibody exists as a isotype IgG, by affinity purification. This antibody has been validated on WB, ELISA.
| Cat.No | ADA-01037A | Clonality | Polyclonal |
|---|---|---|---|
| Host Species | Rabbit | Target Name | SMS |
| Target Synonyms | SRS; SpS; MRSR; SPMSY; MRXSSR; SMS | Form | Liquid |
| Species Reactivity | Human, Mouse | Isotype | IgG |
| Storage Buffer | 50% Glycerol, PBS with 0.01% thimerosal, pH7.3. | Purification Method | Affinity purification |
| Positive Samples | Mouse heart, Mouse kidney, 293T, A375, HT-29, Mouse brain, Raji | Application | ELISA, WB |
| Immunogen Description | Recombinant fusion protein containing a sequence corresponding to amino acids 1-366 of human SMS (NP_004586.2). | Target Species | Human |
|---|---|---|---|
| Uniprot ID | P52788 | Immunogen Sequence |
Uniprot Id
P52788
Target Species
Human
Target Name
SMS
Target Full Name
Spermine synthase
Target Function
Catalyzes the production of spermine from spermidine and decarboxylated S-adenosylmethionine (dcSAM).
Target Involvement
X-linked syndromic mental retardation Snyder-Robinson type (MRXSSR)
Target Protein Families
Spermidine/spermine synthase family
Target Synonyms
MRSR; SMS; Snyder Robinson X linked mental retardation syndrome; Spermidine aminopropyltransferase; Spermine synthase; SPMSY; SpS; SPSY_HUMAN; SRS
Target Background
This gene encodes a protein belonging to the spermidine/spermin synthase family and catalyzes the production of spermine from spermidine. Pseudogenes of this gene are located on chromosomes 1, 5, 6 and X. Mutations in this gene cause an X-linked intellectual disability called Snyder-Robinson Syndrome (SRS). Multiple transcript variants encoding different isoforms have been found for this gene.
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