SMN1 Antibody, ALEXA FLUOR 647

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Catalog number: bs-4628R-A647
Price: 350 €
Supplier: Bioss Primary Conjugated Antibodies
Product name: SMN1 Antibody, ALEXA FLUOR 647
Quantity: 0.1ml
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Long name: ALEXA FLUOR 647 Conjugated, SMN1 Polyclonal Antibody
Also known as: Anti-SMN1 PAb ALEXA FLUOR 647
Category: Conjugated Primary Antibodies
Conjugated with: 647, ALEXA FLUOR®
Host Organism: Rabbit (Oryctolagus cuniculus)
Target Antigen: SMN1
Specificity: This is a highly specific antibody against SMN1
Modification: Unmodified
Modification Site: None
Clonality: Polyclonal
Clone: Polyclonal antibody
Concentration: 1ug per 1ul
Immunogen range: 60-95/294
Source: This antibody was obtained by immunization of the host with KLH conjugated synthetic peptide derived from human SMN1
Gene ID Number: 6606
Tested applications: IF(IHC-P)
Recommended dilutions: IF(IHC-P)(1:50-200)
Crossreactivity: Mouse, Rat, Human
Cross-reactive species details: not every possible cross-reactivity is known, Due to limited amount of testing and knowledge
Background of the antigen: 2a, 2b, Four transcript variants encoding distinct isoforms have been described, It is thought that gene conversion events may involve the two genes, Note that the nine exons of both the telomeric and centromeric copies are designated historically as exon 1, The critical sequence difference between the two genes is a single nucleotide in exon 7, The full length protein encoded by this gene localizes to both the cytoplasm and the nucleus, 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, This duplicated region contains at least four genes and repetitive elements which make it prone to rearrangements and deletions, This gene may be a modifier of disease caused by mutation in the telomeric copy, This protein forms heteromeric complexes with proteins such as SIP1 and GEMIN4, While mutations in the telomeric copy are associated with spinal muscular atrophy, Within the nucleus, and 3-8, and also interacts with several proteins known to be involved in the biogenesis of snRNPs, do not lead to disease, leading to varying copy numbers of each gene, mutations in this gene, such as hnRNP U protein and the small nucleolar RNA binding protein, the centromeric copy, the protein localizes to subnuclear bodies called gems which are found near coiled bodies containing high concentrations of small ribonucleoproteins (snRNPs), which is thought to be an exon splice enhancer, SMN1 is part of a 500 kb inverted duplication on chromosome 5q13
Purification: Purified by Protein A
Storage conditions: 50% glycerol and 0, Keep refrigerated at 2 to 8 degrees Celcius for up to one year, 09% sodium azide, Store this antibody in aqueous buffered solution containing 1% BSA
Excitation emission: 650nm/665nm
Synonyms: BCD541 SMNT SMA1 SMA2 SMA3 GEMIN1 TDRD16A
Properties: ALEXA FLUOR made this Alexa Fluor 633 conjugate that can be used in multi-color flow cytometry with instruments equipped with a second red laser or red diode, ALEXA FLUOR they should be stored frozen at - 24°, Alexa Fluor 633 is a practical alternative to APC as well as Cy5, Bioss Primary Conjugated Antibodies, If you buy Antibodies supplied by Bioss Primary Conjugated Antibodies, It is detected in the FL4 detector of the core's upgraded 2-laser FACScans, Like other Alexa Fluor dyes, exhibits uncommon photo stability, making it an ideal choice for fluorescent microscopy, the SMN1 Antibody, C, C for long term storage and for short term at + 5°, For facs or microscopy Alexa 1 conjugate
Conjugation: ALEXA FLUOR 647, Alexa Fluor
Gene target: SMN1
Short name: SMN1 Antibody
Technique: antibodies against human proteins, antibodies for, Antibody
Label: ALEXA FLUOR 647
Alternative name: ALEXA FLUOR 647, SMN1 (Antibody to)
Alternative technique: antibodies
Identity: 11117
Gene: SMN1 | More about : SMN1
Long gene name: survival of motor neuron 1, telomeric
Synonyms gene: SMA@ SMA
Synonyms gene name: Kugelberg-Welander disease) , spinal muscular atrophy (Werdnig-Hoffmann disease
Synonyms name: gemin-1 tudor domain containing 16A
Locus: 5q13, 2
Discovery year: 1996-12-12
GenBank acession: U18423
Entrez gene record: 6606
Pubmed identfication: 7813012
RefSeq identity: NM_000344
Classification: Tudor domain containing
Havana BLAST/BLAT: OTTHUMG00000099361
Locus Specific Databases: SMN1 - Spinal Muscular Atrophy (SMA) Leiden Muscular Dystrophy pages ALSOD, the Amyotrophic Lateral Sclerosis Online Genetic Database LRG_676

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