You Searched For: Antibodies

Catalog Number: (BOSSBS-4224R-CY3)

Supplier: Bioss

Description: UGT1A9 is a UDP glucuronosyltransferase, an enzyme of the glucuronidation pathway that transforms small lipophilic molecules, such as steroids, bilirubin, hormones, and drugs, into water soluble, excretable metabolites. This gene is part of a complex locus that encodes several UDP glucuronosyltransferases. The locus includes thirteen unique alternate first exons followed by four common exons. Four of the alternate first exons are considered pseudogenes. Each of the remaining nine 5' exons may be spliced to the four common exons, resulting in nine proteins with different N termini and identical C termini. Each first exon encodes the substrate binding site, and is regulated by its own promoter. UGT1A9 is active on phenols.

UOM: 1 * 100 µl

Sale

Catalog Number: (BOSSBS-8223R-CY7)

Supplier: Bioss

Description: FAM155A

UOM: 1 * 100 µl

Sale

Catalog Number: (AVIVARP43993_T100)

Supplier: Aviva Systems Biology

Description: Anti-SLC22A11 Rabbit Polyclonal Antibody

UOM: 1 * 100 µG

Sale

Catalog Number: (AVIVARP40353_P050)

Supplier: Aviva Systems Biology

Description: Anti-CSTF3 Rabbit Polyclonal Antibody

UOM: 1 * 50 µG

Sale

Catalog Number: (AVIVARP40359_T100)

Supplier: Aviva Systems Biology

Description: Anti-EIF4B Rabbit Polyclonal Antibody

UOM: 1 * 100 µG

Sale

Catalog Number: (AVIVARP40368_P050)

Supplier: Aviva Systems Biology

Description: Anti-HNRNPL Rabbit Polyclonal Antibody

UOM: 1 * 50 µG

Sale

Catalog Number: (AVIVARP40373_P050)

Supplier: Aviva Systems Biology

Description: Anti-AUH Rabbit Polyclonal Antibody

UOM: 1 * 50 µG

Sale

Catalog Number: (AVIVARP40379_P050)

Supplier: Aviva Systems Biology

Description: Anti-FMR1 Rabbit Polyclonal Antibody

UOM: 1 * 50 µG

Sale

Catalog Number: (AVIVARP44025_P050)

Supplier: Aviva Systems Biology

Description: Anti-SLC5A7 Rabbit Polyclonal Antibody

UOM: 1 * 50 µG

Sale

Catalog Number: (AVIVARP43438_P050)

Supplier: Aviva Systems Biology

Description: Anti-RNF182 Rabbit Polyclonal Antibody

UOM: 1 * 50 µG

Sale

Catalog Number: (AVIVARP43484_P050)

Supplier: Aviva Systems Biology

Description: Anti-TRIM55 Rabbit Polyclonal Antibody

UOM: 1 * 50 µG

Sale

Catalog Number: (BOSSBS-4239R-FITC)

Supplier: Bioss

Description: Apoptosis-inducing protein that, which can overcome BCL2 suppression. May play a role in repartitioning calcium between the two major intracellular calcium stores in association with BCL2.

UOM: 1 * 100 µl

Sale

Catalog Number: (BOSSBS-11802R-CY7)

Supplier: Bioss

Description: The organic anion transporter family of proteins mediate hepatic uptake of cardiac glycosides. OATP-D is a 710 amino acid member of the organic anion transporter protein family. As a multi-pass membrane protein, OATP-D mediates the Na+-independent transport of vasopressin, prostaglandins (PG) E1 and E2, thyroxine (T4), deltorphin II and other organic anions, but not estrone-3-sulfate, DPDPE, taurocholate, DHEAS or digoxin. OATP-D is ubiquitously expressed with highest levels present in leukocytes and spleen. OATP-D is expressed as four isoforms produced by alternative splicing events.

UOM: 1 * 100 µl

Sale

Catalog Number: (BOSSBS-8289R-CY5)

Supplier: Bioss

Description: Dpy-19 (dumpy-19), is a 683 amino acid C. elegans protein that is required to orient the neuroblasts QL and QR correctly on the anterior/posterior axis. Dpy-19 is expressed highly in dorsal hyp7 cells, ventral P cells and lateral V cells, and dorsal and ventral body muscle cells. DPY19L1 (Dpy-19-like protein 1), also known as KIAA0877, is a 675 amino acid multi-pass membrane protein that belongs to the Dpy-19 family. DPY19L1 is expressed as two isoforms produced by alternative splicing and is encoded by a gene mapping to human chromosome 7, which encodes over 1,000 genes and makes up about 5% of the human genome. Diseases associated with chromosome 7 include Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia.

UOM: 1 * 100 µl

Sale

Catalog Number: (BOSSBS-11555R-CY3)

Supplier: Bioss

Description: The Forkhead-box (FOX) genes comprise a superfamily of at least 43 members that encode proteins which are involved in transcriptional regulation and may be associated with the pathogenesis of various cancers. FOXB1 (forkhead box B1), also known as FKH5 or HFKH-5, and FOXB2 (forkhead box B2) are members of the FOX family and each contain one forkhead DNA-binding domain. Both FOXB1 and FOXB2 localize to the nucleus where they are thought to function as transcription factors that can bind to DNA via their forkhead domains. In mice, defects in the gene encoding FOXB1 are associated with retarded development of the central nervous system (CNS), suggesting that FOXB1 may play a role in CNS organization and function.

UOM: 1 * 100 µl

Sale

Catalog Number: (BOSSBS-1675R-CY5)

Supplier: Bioss

Description: fowl typhoid and pullorum disease

UOM: 1 * 100 µl

Sale