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SMN (Human,Mouse,Rat) Monoclonal antibody
SMN (Human,Mouse,Rat) Monoclonal Antibody for WB, IHC, IF/ICC, ELISA
Host / Isotype
Mouse / IgG2b
Reactivity
human, mouse, rat
Applications
WB, IHC, IF/ICC, ELISA
Conjugate
Unconjugated
CloneNo.
3C10B5
Cat no : 60154-2-Ig
Synonyms
Validation Data Gallery
Tested Applications
Positive WB detected in | HepG2 cells, A375 cells, HeLa cells, T-47D cells, HEK-293 cells, MOLT-4 cells, Jurkat cells, Raji cells |
Positive IHC detected in | mouse liver tissue, mouse brain tissue Note: suggested antigen retrieval with TE buffer pH 9.0; (*) Alternatively, antigen retrieval may be performed with citrate buffer pH 6.0 |
Positive IF/ICC detected in | HepG2 cells |
Recommended dilution
Application | Dilution |
---|---|
Western Blot (WB) | WB : 1:5000-1:50000 |
Immunohistochemistry (IHC) | IHC : 1:500-1:2000 |
Immunofluorescence (IF)/ICC | IF/ICC : 1:400-1:1600 |
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
60154-2-Ig targets SMN (Human,Mouse,Rat) in WB, IHC, IF/ICC, ELISA applications and shows reactivity with human, mouse, rat samples.
Tested Reactivity | human, mouse, rat |
Host / Isotype | Mouse / IgG2b |
Class | Monoclonal |
Type | Antibody |
Immunogen | SMN (Human,Mouse,Rat) fusion protein Ag14333 |
Full Name | survival of motor neuron 2, centromeric |
Calculated Molecular Weight | 282 aa, 30 kDa |
Observed Molecular Weight | 38 kDa |
GenBank Accession Number | BC000908 |
Gene Symbol | SMN |
Gene ID (NCBI) | 6607 |
RRID | AB_10792407 |
Conjugate | Unconjugated |
Form | Liquid |
Purification Method | Protein A purification |
Storage Buffer | PBS with 0.02% sodium azide and 50% glycerol pH 7.3. |
Storage Conditions | Store at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage. 20ul sizes contain 0.1% BSA. |
Background Information
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 | |
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WB protocol for SMN (Human,Mouse,Rat) antibody 60154-2-Ig | Download protocol |
IHC protocol for SMN (Human,Mouse,Rat) antibody 60154-2-Ig | Download protocol |
IF protocol for SMN (Human,Mouse,Rat) antibody 60154-2-Ig | Download protocol |
Standard Protocols | |
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Click here to view our Standard Protocols |