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Anti-C2orf56 (Polyclonal), ALEXA Fluor 594

Anti-C2orf56 (Polyclonal), ALEXA Fluor 594 size: 100 microliters 489

Supplier BIOSS POLYCLONAL ANTIBODIES
Price 489
Size 100 microliters
Contact us Ask Component cell markers and DNA bp. markers are genetic markerser genes or DNA sequenceswith selection audit
TypeConjugated Primary Antibody
Conjugated with 594, ALEXA FLUOR®
Host organismRabbit (Oryctolagus cuniculus)
Target Protein/PeptideC2orf56
SpecificityThis antibody reacts specifically with C2orf56
ModificationNo modification has been applied to this antibody
Modification siteNone
ClonalityPolyclonal Antibody
ClonePolyclonal Antibodies
Concentration1ug per 1ul
Subcellular locationsN/A
Antigen SourceKLH conjugated synthetic peptide derived from human C2orf56
Gene ID55471
Swiss ProtN/A
ApplicationsIF(IHC-P)
Applications with corresponding dilutionsIF(IHC-P)(1:50-200)
Cross reactive species Mouse (Mus musculus), Rat (Rattus norvegicus), Human (Homo sapiens)
Cross Reactive Species details However, note that due to limited knowledge it is impossible to predict with 100% guarantee that the antibody does not corss react with any other species, No significant cross reactivity has been observed for this antibody for the tested species
Background information A number of genetic diseases are linked to genes on chromosome 2, Alstré, An extremely rare recessive genetic disorder, As the second largest human chromosome, C12orf56 is encoded by a gene that maps to human chromosome 2p22, Chromosome 2 contains a probable vestigial second centromere as well as vestigial telomeres, Existing as two alternatively spliced isoforms, Harlequin icthyosis, The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8, a rare skin deformity, also known as PRO1853 or protein midA homolog, chromosome 2 makes up approximately 8% of the human genome and contains 237 million bases encoding over 1, is a 441 amino acid mitochondrial protein that belongs to the midA family, is associated with mutations in the ABCA12 gene, is related to mutations in the ALMS1 gene, syndrome, which are still present in modern day apes, which gives credence to the hypothesis that human chromosome 2 formed as a result of an ancient fusion of two ancestral chromosomes, °, &permil, 2, 400 genes, C12orf56 (chromosome 12 open reading frame 56)
Purification methodPurified by Protein A
Storage 50% glycerol and 0, Store at 4°, 09% sodium azide, C for 12 months, Water buffered solution containing 100ug/ml BSA
Excitation emission590nm/617nm
Synonyms PRO1853 MidA
Also known asC2orf56 Polyclonal Antibody
Other nameAnti-C2orf56 Polyclonal
Advisory For antibodies that are in liquid form or reconstituted lyophilized antibodies small amounts could become entrapped on the seal or the walls of the tube, Prior to use briefly centrifuge the vial to gather all the solution on the bottom, specificity and sensitivity, thus reducing its reactivity, Avoid freeze/thaw cycles as they may denaturate the polypeptide chains of the antibody
PropertiesFor facs or microscopy Alexa 1 conjugate
ConjugationAlexa Fluor
GroupPolyclonals and antibodies
About The advantage is that there are more epitopes available in a polyclonal antiserum to detect the proteins than in monoclonal sera, immunohistochemistry on frozen slices or parrafin fixed tissues, Polyclonals can be used for Western blot
Gene targetC2orf56
Short nameAnti-C2orf56 (Polyclonal) Fluor 594
Technique Pabs are a collection of immunoglobulin , Polyclonal antibodies , each identifying a different , whereas , (pAbs) are mostly rabbit or goat , B cells, Polyclonal, antibodies , antigen, come from a single N cell lineage, epitope, molecules that react against a specific , monoclonal antibodies , that are secreted by different 
LabelALEXA
Alternative name ALEXA Fluor 594, antibody to-C2orf56 (polyclonal)
Alternative techniquepolyclonals
Identity 28816
Gene NDUFAF7
Long gene name NADH:ubiquinone oxidoreductase complex assembly factor 7
Synonyms gene C2orf56
Synonyms gene name assembly factor 7 , chromosome 2 open reading frame 56 NADH dehydrogenase (ubiquinone) complex I
Synonyms name mitochondrial dysfunction protein A homolog
Locus 2p22, 2
Discovery year 2007-05-31
Entrez gene record 55471
RefSeq identity NM_144736
Classification Mitochondrial respiratory chain complex assembly factors
Havana BLAST/BLAT OTTHUMG00000128468

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