BBS5 Recombinant monoclonal antibody, PBS Only (Detector) 83722-1-PBS proteintech

$699.00
In stock
SKU
83722-1-PBS
Catalog No.SizePrice (USD)
83722-1-PBS-100UG100 μg$699.00
Catalog Number83722-1-PBS
Synonyms240674B5, Bardet Biedl syndrome 5, Bardet-Biedl syndrome 5 protein
HostRabbit
Reactivityhuman, mouse, rat
FormLiquid
FormulationPBS Only
ApplicationsWB, IF/ICC, Cytometric bead array, Indirect ELISA
Host / IsotypeRabbit / IgG
Tested Reactivityhuman, mouse, rat
ClassRecombinant
TypeAntibody
ImmunogenCatNo: Ag6153 Product name: Recombinant human BBS5 protein Source: e coli. -derived, PGEX-4T Tag: GST Domain: 1-341 aa of BC044593 Sequence: MSVLDALWEDRDVRFDLSAQQMKTRPGEVLIDCLDSIEDTKGNNGDRGRLLVTNLRILWHSLALSRVNVSVGYNCILNITTRTANSKLRGQTEALYILTKCNSTRFEFIFTNLVPGSPRLFTSVMAVHRAYETSKMYRDFKLRSALIQNKQLRLLPQEHVYDKINGVWNLSSDQGNLGTFFITNVRIVWHANMNDSFNVSIPYLQIRSIKIRDSKFGLALVIESSQQSGGYVLGFKIDPVEKLQESVKEINSLHKVYSASPIFGVDYEMEEKPQPLEALTVEQIQDDVEIDSDGHTDAFVAYFADGNKQQDREPVFSEELGLAIEKLKDGFTLQGLWEVMS Predict reactive species
Full NameBardet-Biedl syndrome 5
Calculated Molecular Weight39 kDa
Observed Molecular Weight39 kDa
GenBank Accession NumberBC044593
Gene SymbolBBS5
Gene ID (NCBI)129880
RRIDAB_3671323
ConjugateUnconjugated
Purification MethodProtein A purification
UNIPROT IDQ8N3I7
Storage BufferPBS only, pH 7.3.
Storage ConditionsStore at -80°C.
Citations-
IsotypeIgG
ClonalityRecombinant
Clone Number240674B5
ConjugationUnconjugated

BBS5 encodes a protein that has been directly linked to Bardet-Biedl syndrome. Bardet-Biedl syndrome (BBS) is an autosomal recessive condition characterised by rod-cone dystrophy, postaxial polydactyly, central obesity, mental retardation, hypogonadism, and renal dysfunction. Other associated clinical findings in BBS patients include diabetes, hypertension and congenital heart defects. BBS expression varies both within and between families and diagnosis is often difficult. Experimentation in non-human eukaryotes suggests that BBS5 is expressed in ciliated cells and that it is required for the formation of cilia. Alternate transcriptional splice variants have been observed but have not been fully characterized.

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