Gemin 3/SMA Antibody, Cy5 Conjugated

Catalog number:	bs-11563R-Cy5 Buy Now
Price:	332 €
Supplier:	Bioss Primary Conjugated Antibodies.
Product name:	Gemin 3/SMA Antibody, Cy5 Conjugated
Quantity:	100ul
Related search:	gemin sma antibody gene conjugated synonyms disease neuron

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Long name:	Cy5 Conjugated, Gemin 3/SMA Polyclonal Antibody
Category:	Conjugated Primary Antibodies
Conjugation:	5, Cy5
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:	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
Crossreactive species details:	not every possible cross-reactivity is known, Due to limited amount of testing and knowledge
Antigen background:	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 method:	This antibody was purified via Protein A
Storage conditions:	50% glycerol and 0, Store refrigerated at 2 to 8 degrees Celcius for up to 1 year, 09% sodium azide, Keep the antibody in an aqueous buffered solution containing 1% BSA
Excitation Emission:	625, 650nm/670nm
Synonyms:	BCD541 SMNT SMA1 SMA2 SMA3 GEMIN1 TDRD16A
Properties:	Cy5 antibodies are excited by the 650-nanometer wave of an argon laser and detected at a 670-nanometer captor, C, C for long term storage and for short term at + 5°, If you buy Antibodies supplied by Bioss Primary Conjugated Antibodies they should be stored frozen at - 24°
Gene target:	Gemin 3/SMA Conjugated
Short name:	Conjugated, Gemin 3/SMA Antibody
Technique:	antibodies against human proteins, antibodies for, antibody Conjugates, Antibody
Label:	Cy5
Alternative name:	cyanine 5 coupled, 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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