41249 Results for: "Iodic+acid&pageNo=67"

Supplier: Abcam

Rabbit monoclonal [EPR25804-63] to TIGIT - BSA and Azide free (Capture).

Supplier: Abcam

Rabbit monoclonal [EPR11203-27] to C4b - BSA and Azide free.

Supplier: Abcam

Rabbit monoclonal [EPR25616-62] to CD62E - BSA and Azide free.

Supplier: Abcam

Rabbit monoclonal [EPR26134-17] to Jagged1 - BSA and Azide free.

Supplier: Abcam

Rabbit monoclonal [EPR18133-57] to RhoA - BSA and Azide free (Capture).

Supplier: Abcam

Rabbit monoclonal [EPR26466-37] to Seladin 1 - BSA and Azide free.

Supplier: Abcam

Rabbit monoclonal [EPR24506-61] to IRAK4 - BSA and Azide free (Capture).

Supplier: Abcam

Rabbit monoclonal [EPR25413-65] to ATF3 - BSA and Azide free.

Supplier: Abcam

Rabbit monoclonal [EPR27244-57] to MSH4 - BSA and Azide free.

Supplier: Abcam

Rabbit monoclonal [EPR27258-37] to LAMA1 - BSA and Azide free.

Supplier: Abcam

Rabbit monoclonal [EPR27180-62] to Neurotensin - BSA and Azide free.

Supplier: Abcam

Rabbit monoclonal [EPR26969-66] to CLEC4A - BSA and Azide free (Capture).

Supplier: Abcam

Rabbit monoclonal [EPR26530-17] to CD40L - BSA and Azide free.

Supplier: Apollo Scientific

9,9-Dimethylfluorene-2,7-diboronic acid bis(pinacol) ester

Supplier: Bioss

This gene encodes a secreted chemotactic protein that initiates chemotaxis via the ChemR23 G protein-coupled seven-transmembrane domain ligand. Expression of this gene is upregulated by the synthetic retinoid tazarotene and occurs in a wide variety of tissues. The active protein has several roles, including that as an adipokine, and is truncated on both termini from the proprotein.

Supplier: Bioss

CCDC112, also known as MBC1 (mutated in bladder cancer 1), is a 446 amino acid protein. The gene encoding CCDC112 is located on chromosome 5. Due to alternative splicing events, CCDC112 exists as two isoforms. Chromosome 5 comprises about 6% of human genomic DNA and contains 181 million base pairs encoding around 1,000 genes. It is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome

Supplier: Apollo Scientific

3-(Boc-amino)-6,6-dichlorobicyclo[3.1.0]hexane-3-carboxylic acid

Supplier: Bioss

ZNF420 contains 19 C2H2-type zinc fingers and 1 KRAB domain. It may be involved in transcriptional regulation. It is a negative regulator of p53-mediated apoptosis.

Supplier: Bioss

The SHC gene encodes for a signaling and transforming protein containing Src homology 2 and 3 (SH2 and SH3) domains. The SHC gene encodes 2 widely expressed overlapping proteins of 46 and 52 kD, both containing a C-terminal SH2 domain. Adjacent to the SH2 region is a glycine and proline rich region. These 2 proteins differ in their N terminals. SHC proteins are involved in mitogenic signal transduction and act by coupling growth factor receptors to the RAS signaling pathway. The protein encoded by the SHC1 gene is thought to act as an adaptor in many signal transduction pathways.

Supplier: Bioss

DPPA5 is a 116 amino acid protein that localizes to the cytoplasm and contains one KH domain. Expressed in embryonic germ (EG), primordial germ (PG) and embryonic stem (ES) cells, DPPA5 plays an important role in the maintenance of ES cell pluripotency and may be necessary for proper embryogenesis. The gene encoding DPPA5 maps to human chromosome 6, which contains 170 million base pairs and comprises nearly 6% of the human genome. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer, suggesting the presence of a cancer susceptibility locus. Additionally, Porphyria cutanea tarda, Parkinson's disease, Stickler syndrome and a susceptibility to bipolar disorder are all associated with genes that map to chromosome 6.

Supplier: Bioss

This gene encodes a protein which is a member of the bromodomain-containing protein family. The product of this gene has been identified as a component of one form of the SWI/SNF chromatin remodeling complex, and as a protein which interacts with p53 and is required for p53-dependent oncogene-induced senescence which prevents tumor growth. Pseudogenes have been described on chromosomes 2, 3, 6, 13 and 14. Alternative splicing results in multiple transcript variants.

Supplier: Bioss

Necessary for the biosynthesis of the Pk antigen of blood histogroup P. Catalyzes the transfer of galactose to lactosylceramide and galactosylceramide. Necessary for the synthesis of the receptor for bacterial verotoxins.

Supplier: Bioss

Chromosome 7 has been linked to 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 characterised 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. The C7orf57 gene product has been provisionally designated C7orf57 pending further characterisation.

Supplier: Bioss

mTOR controls cell growth, in part by regulating p70 S6 kinase alpha (p70alpha) and eukaryotic initiation factor 4E binding protein 1 (4EBP1). Raptor is a 150 kDa mTOR binding protein that also binds 4EBP1 and p70alpha. The binding of Raptor to mTOR is necessary for the mTOR-catalyzed phosphorylation of 4EBP1 in vitro, and it strongly enhances the mTOR kinase activity toward p70alpha. Rapamycin or amino acid withdrawal increases, whereas insulin strongly inhibits, the recovery of 4EBP1 and raptor on 7-methyl-GTP Sepharose. Partial inhibition of raptor expression by RNA interference (RNAi) reduces mTOR-catalyzed 4EBP1 phosphorylation in vitro. RNAi of C. elegans raptor yields an array of phenotypes that closely resemble those produced by inactivation of Ce-TOR. Thus, raptor is an essential scaffold for the mTOR-catalyzed phosphorylation of 4EBP1 and mediates TOR action in vivo.

Supplier: Bioss

In cooperation with other chaperones, Hsp70s stabilize preexistent proteins against aggregation and mediate the folding of newly translated polypeptides in the cytosol as well as within organelles. These chaperones participate in all these processes through their ability to recognize nonnative conformations of other proteins. They bind extended peptide segments with a net hydrophobic character exposed by polypeptides during translation and membrane translocation, or following stress-induced damage. Sequence similarities Belongs to the heat shock protein 70 family.

Supplier: Bioss

C5orf22

Supplier: Apollo Scientific

1-{2,7-Diazaspiro[3.5]nonan-7-yl}ethan-1-one hydrochloride

Supplier: Abcam

Rabbit monoclonal [EPR16610-69] to IL-6 - BSA and Azide free.

Supplier: Abcam

Rabbit monoclonal [EPR20445-61] to BTK - BSA and Azide free (Capture).

Supplier: Abcam

Rabbit monoclonal [EPR23075-57] to NRG1 - BSA and Azide free (Capture).