The SMN2 Polyclonal Antibody (CAB1652) is a valuable tool for researchers studying SMN2, a gene involved in spinal muscular atrophy (SMA), a genetic disorder that affects the motor neurons in the spinal cord. This antibody, raised in rabbits, is highly specific to human samples and has been validated for use in Western blot applications.The SMN2 Polyclonal Antibody binds specifically to the SMN2 protein, allowing for the detection and analysis of this critical gene in various cell types. By using this antibody, researchers can gain a better understanding of the role that SMN2 plays in the development of SMA and potentially discover new therapeutic targets for the treatment of this devastating disease.
Overall, the SMN2 Polyclonal Antibody is a valuable tool for researchers studying SMA and seeking to uncover new insights into the molecular mechanisms underlying this disorder. Its high specificity and reliability make it an excellent choice for studies focused on understanding the pathophysiology of SMA and developing novel therapies for this condition.
Product Name:
SMN2 Rabbit Polyclonal Antibody
SKU:
CAB1652
Size:
20uL, 100uL
Isotype:
IgG
Host Species:
Rabbit
Reactivity:
Human,Mouse,Rat
Immunogen:
Recombinant fusion protein containing a sequence corresponding to amino acids 1-197 of human SMN2 (NP_059107.1).
This gene is part of a 500 kb inverted duplication on chromosome 5q13. This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions. The repetitiveness and complexity of the sequence have also caused difficulty in determining the organization of this genomic region. The telomeric and centromeric copies of this gene are nearly identical and encode the same protein. While mutations in the telomeric copy are associated with spinal muscular atrophy, mutations in this gene, the centromeric copy, do not lead to disease. This gene may be a modifier of disease caused by mutation in the telomeric copy. The critical sequence difference between the two genes is a single nucleotide in exon 7, which is thought to be an exon splice enhancer. Note that the nine exons of both the telomeric and centromeric copies are designated historically as exon 1, 2a, 2b, and 3-8. It is thought that gene conversion events may involve the two genes, leading to varying copy numbers of each gene. The full length protein encoded by this gene localizes to both the cytoplasm and the nucleus. Within the nucleus, the protein localizes to subnuclear bodies called gems which are found near coiled bodies containing high concentrations of small ribonucleoproteins (snRNPs). This protein forms heteromeric complexes with proteins such as SIP1 and GEMIN4, and also interacts with several proteins known to be involved in the biogenesis of snRNPs, such as hnRNP U protein and the small nucleolar RNA binding protein. Four transcript variants encoding distinct isoforms have been described.
Purification Method:
Affinity purification
Gene ID:
6607
Storage Buffer:
Store at -20℃. Avoid freeze / thaw cycles.Buffer: PBS with 0.02% sodium azide,50% glycerol,pH7.3.
Western blot analysis of various lysates using SMN2 Rabbit pAb (CAB1652) at 1:1000 dilution.Secondary antibody: HRP Goat Anti-Rabbit IgG (H+L) (CABS014) at 1:10000 dilution.Lysates/proteins: 25μg per lane.Blocking buffer: 3% nonfat dry milk in TBST.Detection: ECL Basic Kit (AbGn00020).Exposure time: 30s.
