Ile Czasu Zajmuje Test Na Przeciwciala Igm I Igg Na Borelioze

Description: Solid 96 well plates NEUTRAVIDIN COATED Color:White blocking:Standard

Description: 96 well plates - 12x8 Well Breakable Strips on single well holding frame NEUTRAVIDIN COATED Color:Clear blocking:Standard

Description: 96 well plates - 12x8 Well Breakable Strips on single well holding frame NEUTRAVIDIN COATED Color:Black blocking:Standard

Description: 96 well plates - 12x8 Well Breakable Strips on single well holding frame NEUTRAVIDIN COATED Color:White blocking:Standard

Description: Rabbit polyclonal to Na+ CP type IIalpha.

Description: Rabbit polyclonal to Na+ CP type IIalpha.

Description: Rabbit polyclonal to Na+ CP type IIbeta.

Description: Rabbit polyclonal to Na+ CP type IValpha.

Description: Rabbit polyclonal to Na+ CP type IXalpha.

Description: Method of detection: Coated with Antigen, Competitive ELISA;Reacts with: General;Sensitivity: 9.375pg/ml

Description: This gene is a member of the telombin family and encodes a nuclear protein involved in telomere maintenance. Specifically, this protein functions as a member of a multi-protein complex that binds to the TTAGGG repeats of telomeres, regulating telomere length and protecting chromosome ends from illegitimate recombination, catastrophic chromosome instability, and abnormal chromosome segregation. Increased transcriptional expression of this gene is associated with stomach carcinogenesis and its progression. Alternatively spliced transcript variants have been described.

Description: The protein encoded by this gene belongs to the Rab family of the small GTPase superfamily. It is associated with both constitutive and regulated secretory pathways, and may be involved in protein transport. Two transcript variants encoding different isoforms have been found for this gene.

Description: This gene encodes a pyrin-like protein containing a pyrin domain, a nucleotide-binding site (NBS) domain, and a leucine-rich repeat (LRR) motif. This protein interacts with the apoptosis-associated speck-like protein PYCARD/ASC, which contains a caspase recruitment domain, and is a member of the NALP3 inflammasome complex. This complex functions as an upstream activator of NF-kappaB signaling, and it plays a role in the regulation of inflammation, the immune response, and apoptosis. Mutations in this gene are associated with familial cold autoinflammatory syndrome (FCAS), Muckle-Wells syndrome (MWS), chronic infantile neurological cutaneous and articular (CINCA) syndrome, and neonatal-onset multisystem inflammatory disease (NOMID). Multiple alternatively spliced transcript variants encoding distinct isoforms have been identified for this gene. Alternative 5' UTR structures are suggested by available data; however, insufficient evidence is available to determine if all of the represented 5' UTR splice patterns are biologically valid.

Description: This gene encodes a membrane-bound protein which is a member of the ELO family, proteins which participate in the biosynthesis of fatty acids. Consistent with the expression of the encoded protein in photoreceptor cells of the retina, mutations and small deletions in this gene are associated with Stargardt-like macular dystrophy (STGD3) and autosomal dominant Stargardt-like macular dystrophy (ADMD), also referred to as autosomal dominant atrophic macular degeneration.