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C11orf24 Antibody, ALEXA FLUOR 594

C11orf24 Antibody, ALEXA FLUOR 594 size: 100ul 332

Supplier BIOSS PRIMARY CONJUGATED ANTIBODIES
Price 332
Size 100ul
Contact us Ask Component cell markers and DNA bp. markers are genetic markerser genes or DNA sequenceswith selection audit
Long name ALEXA FLUOR 594 Conjugated, C11orf24 Polyclonal Antibody
Also known asAnti-C11orf24 PAb ALEXA FLUOR 594
CategoryConjugated Primary Antibodies
Conjugated with 594, ALEXA FLUOR®
Host OrganismRabbit (Oryctolagus cuniculus)
Target AntigenC11orf24
SpecificityThis is a highly specific antibody against C11orf24
ModificationUnmodified
Modification SiteNone
ClonalityPolyclonal
ClonePolyclonal antibody
Concentration1ug per 1ul
Subcellular locationExtracellular
SourceThis antibody was obtained by immunization of the host with KLH conjugated synthetic peptide derived from human C11orf24
Gene ID Number53838
Tested applicationsIF(IHC-P)
Recommended dilutionsIF(IHC-P)(1:50-200)
CrossreactivityHuman
Cross-reactive species details not every possible cross-reactivity is known, Due to limited amount of testing and knowledge
Background of the antigen Atm mutation leads to the disorder known as ataxia-telangiectasia, C11orf24 is encoded by a gene located on human chromosome 11, Chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome, Jacobsen syndrome, Jervell and Lange-Nielsen syndrome, Niemann-Pick disease, The blood disorders Sickle cell anemia and Î, The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene, Wilms' tumors, also known as DM4E3, and low expression in thymus and leukocytes, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11, is a 449 amino acid single-pass type I membrane protein that is expressed in brain, kidney, liver, lung, ovary and small intestine, pancreas and colon, placenta, prostate, skeletal muscle, spleen, testis, thalassemia are caused by HBB gene mutations, which consists of approximately 135 million base pairs and 1, with highest expression in heart, ², 400 genes, C11orf24
PurificationPurified 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 emission590nm/617nm
Synonyms DM4E3
Properties ALEXA FLUOR they should be stored frozen at - 24°, If you buy Antibodies supplied by Bioss Primary Conjugated Antibodies, C, C for long term storage and for short term at + 5°, For facs or microscopy Alexa 1 conjugate
Conjugation 594, ALEXA FLUOR®, Alexa Fluor
ConjugatedAlexa conjugate 1
Gene targetC11orf24
Short nameC11orf24 Antibody
Technique antibodies against human proteins, antibodies for, Antibody
LabelALEXA FLUOR 594
Alternative name ALEXA FLUOR 594, C11orf24 (Antibody to)
Alternative techniqueantibodies
Identity 1174
Gene C11orf24
Long gene name chromosome 11 open reading frame 24
Locus 11q13, 2
Discovery year 2000-05-23
GenBank acession AF264781
Entrez gene record 53838
Pubmed identfication 11401438 24312644
RefSeq identity NM_022338
Havana BLAST/BLAT OTTHUMG00000167478

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