CoraLite®594-conjugated SMN (Human,Mouse,Rat) Monoclonal antibody CL594-60154 proteintech

$479.00
In stock
SKU
CL594-60154
Catalog No.SizePrice (USD)
CL594-60154-100UL100 μL$479.00
Catalog NumberCL594-60154
SynonymsC BCD541, Component of gems 1, FLJ76644, Gemin 1, SMN, SMN (Human,Mouse,Rat), SMN1, SMN1,SMN, SMN2, SMNC, SMNT, Survival motor neuron protein
HostMouse
Reactivityhuman, mouse, rat
FormLiquid
FormulationPBS, Proclin300, BSA, Glycerol
ApplicationsIF/ICC
Host / IsotypeMouse / IgG2b
Tested Applications — Positive IF/ICC detected inHepG2 cells
Recommended Dilutions — Immunofluorescence (IF)/ICCIF/ICC : 1:50-1:500
Positive IF/ICC detected inHepG2 cells
Immunofluorescence (IF)/ICCIF/ICC : 1:50-1:500
Tested Reactivityhuman, mouse, rat
ClassMonoclonal
TypeAntibody
ImmunogenCatNo: Ag14333 Product name: Recombinant human SMN2 protein Source: e coli. -derived, PET28a Tag: 6*His Domain: 1-282 aa of BC000908 Sequence: MAMSSGGSGGGVPEQEDSVLFRRGTGQSDDSDIWDDTALIKAYDKAVASFKHALKNGDICETSGKPKTTPKRKPAKKNKSQKKNTAASLQQWKVGDKCSAIWSEDGCIYPATIASIDFKRETCVVVYTGYGNREEQNLSDLLSPICEVANNIEQNAQENENESQVSTDESENSRSPGNKSDNIKPKSAPWNSFLPPPPPMPGPRLGPGKPGLKFNGPPPPPPPPPPHLLSCWLPPFPSGPPIIPPPPPICPDSLDDADALGSMLISWYMSGYHTGYYMEMLA Predict reactive species
Full Namesurvival of motor neuron 2, centromeric
Calculated Molecular Weight282 aa, 30 kDa
Observed Molecular Weight38 kDa
GenBank Accession NumberBC000908
Gene SymbolSMN
Gene ID (NCBI)6607
RRIDAB_2883429
ConjugateCoraLite®594 Fluorescent Dye
Excitation/Emission Maxima Wavelengths588 nm / 604 nm
Excitation LaserYellow-Green Laser (561 nm)
Purification MethodProtein A purification
UNIPROT IDQ16637
Storage BufferPBS with 50% glycerol, 0.05% Proclin300, 0.5% BSA, pH 7.3.
Storage ConditionsStore at -20°C. Avoid exposure to light. Stable for one year after shipment. Aliquoting is unnecessary for -20 o C storage.
IF protocol for CL594 SMN (Human,Mouse,Rat) antibody CL594-60154Download protocol
Citations-
DilutionsIF/ICC : 1:50-1:500
IsotypeIgG2b
ClonalityMonoclonal
Clone Number3C10B5
ConjugationCoraLite®594

The survival of motor neurons (SMN) genes are the disease genes of spinal muscular atrophy (SMA), a common motor neuron degenerative disease. The level of SMN protein correlates with phenotypic severity of SMA. SMA patients lack a functional SMN1 gene, but they possess an intact SMN2 gene, which though nearly identical to SMN1, is only partially functional, because a large majority of SMN2 transcripts lack exon 7, resulting in production of a truncated, less stable SMN protein. This antibody 60154-2-Ig can recognize human,mouse and rat SMN gene. Protocols Product Specific Protocols IF protocol for CL594 SMN (Human,Mouse,Rat) antibody CL594-60154 Download protocol Standard Protocols Click here to view our Standard Protocols

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