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Ace+Method+Development+Kits
Catalog Number:
(10104-750)
Supplier:
Prosci
Description:
The Fos gene family consists of 4 members: FOS, FOSB, FOSL1, and FOSL2, which encode leucine zipper proteins that can dimerize with proteins of the JUN family, thereby forming the transcription factor complex AP-1. The FOS proteins have been implicated as regulators of cell proliferation, differentiation, and transformation.
Catalog Number:
(10102-086)
Supplier:
Prosci
Description:
HBP1 is a transcriptional repressor that binds to the promoter region of target genes. This protein plays a role in the regulation of the cell cycle and of the Wnt pathway. It binds preferentially to the sequence 5'-TTCATTCATTCA-3'. Binding to the H1F0 promoter, HBP1 is enhanced by interaction with RB1. The protein also can disrupt the interaction between DNA and TCF4.
Catalog Number:
(10100-708)
Supplier:
Prosci
Description:
GFI1 may be a transcription factor involved in regulating the expression of genes active in the S phase during cell cycle progression in T-cells. GFI1 may be involved in tumor progression. Defects in GFI1 are a cause of autosomal dominant severe congenital neutropenia (SCN) and dominant nonimmune chronic idiopathic neutropenia of adults (NI-CINA)
Catalog Number:
(10110-830)
Supplier:
Prosci
Description:
TIP39 is related to parathyroid hormone (PTH) and PTH-related protein (PTHRP) and is a ligand for PTH receptor-2.TIP39 is related to parathyroid hormone (PTH; MIM 168450) and PTH-related protein (PTHRP; MIM 168470) and is a ligand for PTH receptor-2 (PTHR2; MIM 601469) (John et al., 2002 [PubMed 11861531]).
Catalog Number:
(CAAAB22235-01)
Catalog Number:
(CA1.02711.0250)
Supplier:
MilliporeSigma
Description:
Copper(II) acetate monohydrate, EMSURE® ACS for analysis, Supelco®
Catalog Number:
(10105-188)
Supplier:
Prosci
Description:
HES1 belongs to the basic helix-loop-helix family of transcription factors. It is a transcriptional repressor of genes that require a bHLH protein for their transcription. The protein has a particular type of basic domain that contains a helix interrupting protein that binds to the N-box rather than the canonical E-box.
Catalog Number:
(10099-944)
Supplier:
Prosci
Description:
ChGn transfers 1,4-N-acetylgalactosamine (GalNAc) from UDP-GalNAc to the non-reducing end of glucuronic acid (GlcUA). This protein is required for addition of the first GalNAc to the core tetrasaccharide linker and for elongation of chondroitin chains. It play an important role in chondroitin chain biosynthesis in cartilage.
Catalog Number:
(10101-658)
Supplier:
Prosci
Description:
SUPT5H and its binding partner regulate transcriptional elongation by RNA polymerase II. SPT4 and SPT5 are involved in both 5,6-dichloro-1-beta-D-ribofuranosylbenzimidazole (DRB)-mediated transcriptional inhibition and the activation of transcriptional elongation by the human immunodeficiency virus type 1 (HIV-1) Tat protein.
Catalog Number:
(10104-316)
Supplier:
Prosci
Description:
The function of C2orf25 remains unknown.Vitamin B12 (cobalamin) is an essential cofactor in several metabolic pathways. Intracellular conversion of cobalamin to adenosylcobalamin in mitochondria and to methylcobalamin in cytoplasm is necessary for homeostasis of methylmalonic acid and homocysteine. C2ORF25 encodes a protein involved in an early step of cobalamin metabolism (Coelho et al., 2008 [PubMed 18385497]).
Catalog Number:
(CA111-1101)
Supplier:
Rockland Immunochemical
Description:
Anti-Rabbit serum antibody is suitable for western blotting, IP and for ELISA. Researchers should determine optimal titers for applications that are not stated below.
Catalog Number:
(103360-568)
Supplier:
Novus Biologicals
Description:
The NIFK Antibody (18E148) [DyLight 405] from Novus Biologicals is a mouse monoclonal antibody to NIFK. This antibody reacts with human. The NIFK Antibody (18E148) [DyLight 405] has been validated for the following applications: Western Blot.
Catalog Number:
(10099-714)
Supplier:
Prosci
Description:
DGCR8 contains 2 DRBM (double-stranded RNA-binding) domains and 1 WW domain. It may play a part in the etiology of the velocardiofacial/DiGeorge syndrome (VCFS/DGS), a developmental disorder characterized by structural and functional palate anomalies, conotruncal cardiac malformations, immunodeficiency, hypocalcemia, and typical facial anomalies.
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