Gemin 3/SMA Antibody, ALEXA FLUOR 647

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Catalog number: bs-11563R-A647
Price: 332 €
Supplier: Bioss Primary Conjugated Antibodies.
Product name: Gemin 3/SMA Antibody, ALEXA FLUOR 647
Quantity: 100ul
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Long name: ALEXA FLUOR 647 Conjugated, Gemin 3/SMA Polyclonal Antibody
Also known as: Anti-Gemin 3/SMA PAb ALEXA FLUOR 647
Category: Conjugated Primary Antibodies
Conjugated with: 647, ALEXA FLUOR®
Host Organism: Rabbit (Oryctolagus cuniculus)
Target Antigen: Gemin 3/SMA
Specificity: This is a highly specific antibody against Gemin 3/SMA
Modification: Unmodified
Modification Site: None
Clonality: Polyclonal
Clone: Polyclonal antibody
Concentration: 1ug per 1ul
Source: This antibody was obtained by immunization of the host with KLH conjugated synthetic peptide derived from human Gemin 3
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: DDX20, DEAD-box protein DP130 and DEAD/H box 20, Gemin3, Gemin3 also interacts with SmB, Gemin3 is a putative RNA helicase and shows ATPase activity, Gemin4, Gemin5 and Gemin6, It associates directly with SMN and is a part of the SMN complex containing Gemin2, It contains the conserved motif Asp-Glu-Ala-Asp (DEAD) characteristic of DEAD-box proteins, It is expressed in B and T cell neuroblastoma-derived cell lines, It is found in both the cytoplasm and the nucleus, SMA is caused by deletion or loss-of-function mutations in the SMN (survival of motor neuron) gene, SmD2 and SmD3, The SMN complex plays an essential role in spliceosomal snRNP assembly in the cytoplasm and is required for pre-mRNA splicing of the nucleus, The nuclear form is concentrated in subnuclear bodies called gems (for Gemini of the coiled bodies), also known as DP103, as well as several spliceosomal snRNP proteins, is a protein product of human chromosome 1p13, kidney and lung, liver, malignant melanoma tumor, normal testis and is expressed in low levels in colon, skeletal muscle, 2, Spinal muscular atrophy (SMA) is an autosomal recessive neurodegenerative disease characterized by loss of motor neurons in the spinal cord
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 Gemin 3/SMA 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: Gemin 3/SMA
Short name: Gemin 3/SMA Antibody
Technique: antibodies against human proteins, antibodies for, Antibody
Label: ALEXA FLUOR 647
Alternative name: ALEXA FLUOR 647, Gemin 3/SMA (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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