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Anti-MPPED2/Brain protein 239, ALEXA Fluor 594

Anti-MPPED2/Brain protein 239, 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/PeptideMPPED2/Brain protein 239
SpecificityThis antibody reacts specifically with MPPED2/Brain protein 239
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 MPPED2/Brain protein 239
Gene IDN/A
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 Atm mutation leads to the disorder known as ataxia-telangiectasia, Expressed primarily in fetal brain tissue, FAM1B or 239FB, Jacobsen syndrome, Jervell and Lange-Nielsen syndrome, MPPED2 is encoded by a gene that maps to chromosome 11, Niemann-Pick disease, The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations, The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double stranded DNA breaks, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene, With approximately 135 million base pairs and 1, also known as C11orf8, chromosome 11 makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11, is a 294 amino acid protein, while Wilms' tumors, 400 genes, MPPED2 (Metallophosphoesterase domain-containing protein 2)
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 239FB D11S302E Hs, 1 , 1 dJ1024C24, 46638 FAM1B dJ873F21
Also known asMPPED2/Brain protein 239 Antibody
Other nameAnti-MPPED2/Brain protein 239
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
Gene targetMPPED2/Brain protein 239
Short name Fluor 594, Anti-MPPED2/Brain protein 239
LabelALEXA
Alternative name ALEXA Fluor 594, antibody to-MPPED2/Brain protein 239
Identity 1180
Gene MPPED2
Long gene name metallophosphoesterase domain containing 2
Synonyms gene C11orf8
Synonyms gene name chromosome 11 open reading frame 8
Locus 11p14, 1
Discovery year 1998-08-06
GenBank acession U57911
Entrez gene record 744
Pubmed identfication 8666403 9266672
RefSeq identity NM_001584
Havana BLAST/BLAT OTTHUMG00000166159

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