Votre recherche pour: 521-1646

Numéro de catalogue: (BOSSBS-3608R-A750)

Fournisseur: Bioss

Description: This gene encodes a member of the cytochrome P450 superfamily of enzymes. The cytochrome P450 proteins are monooxygenases which catalyse many reactions involved in drug metabolism and synthesis of cholesterol, steroids and other lipids. This protein localises to the mitochondrial inner membrane and catalyses the conversion of cholesterol to pregnenolone, the first and rate-limiting step in the synthesis of the steroid hormones. Two transcript variants encoding different isoforms have been found for this gene. The cellular location of the smaller isoform is unclear since it lacks the mitochondrial-targeting transit peptide.

UOM: 1 * 100 µl

Promotion

Numéro de catalogue: (ACRBCD7-C52H9100UG)

Fournisseur: ACROBIOSYSTEMS

Description: CD117 / C-KIT CYNO HIS 1 * 100 µG

UOM: 1 * 1 EA

Promotion

 Il s'agit d'un élément MarketSource. Des frais supplémentaires peuvent s'appliquer.

Numéro de catalogue: (BOSSBS-4136R-A680)

Fournisseur: Bioss

Description: Transcriptional activator which binds specifically to the MEF2 element, 5'-YTA[AT](4)TAR-3', found in numerous muscle-specific, growth factor- and stress-induced genes. Mediates cellular functions not only in skeletal and cardiac muscle development, but also in neuronal differentiation and survival. Plays diverse roles in the control of cell growth, survival and apoptosis via p38 MAPK signaling in muscle-specific and/or growth factor-related transcription. Plays a critical role in the regulation of neuronal apoptosis (By similarity).

UOM: 1 * 100 µl

Promotion

Numéro de catalogue: (BOSSBS-4136R-A750)

Fournisseur: Bioss

Description: Transcriptional activator which binds specifically to the MEF2 element, 5'-YTA[AT](4)TAR-3', found in numerous muscle-specific, growth factor- and stress-induced genes. Mediates cellular functions not only in skeletal and cardiac muscle development, but also in neuronal differentiation and survival. Plays diverse roles in the control of cell growth, survival and apoptosis via p38 MAPK signaling in muscle-specific and/or growth factor-related transcription. Plays a critical role in the regulation of neuronal apoptosis (By similarity).

UOM: 1 * 100 µl

Promotion

Numéro de catalogue: (ABNOH00084668-P01)

Fournisseur: Abnova

Description: FAM126A RECOMBINANT PROTEIN (P01) 1 * 2 µG

UOM: 1 * 2 µG

Promotion

Numéro de catalogue: (ABNOH00084364-P01)

Fournisseur: Abnova

Description: ZNF289 RECOMBINANT PROTEIN (P01) 1 * 2 µG

UOM: 1 * 2 µG

Promotion

Numéro de catalogue: (ABNOH00001583-Q012)

Fournisseur: Abnova

Description: CYP11A1 (HUMAN) RECOMBINANT PROTEIN (Q01 1 * 25 µG

UOM: 1 * 25 µG

Promotion

Numéro de catalogue: (ABNOH00009113-Q012)

Fournisseur: Abnova

Description: LATS1 (HUMAN) RECOMBINANT PROTEIN (Q01) 1 * 25 µG

UOM: 1 * 25 µG

Promotion

Numéro de catalogue: (ABNOH00010592-Q012)

Fournisseur: Abnova

Description: SMC2L1 (HUMAN) RECOMBINANT PROTEIN (Q01) 1 * 25 µG

UOM: 1 * 25 µG

Promotion

Numéro de catalogue: (ABNOH00004600-Q012)

Fournisseur: Abnova

Description: MX2 (HUMAN) RECOMBINANT PROTEIN (Q01) 1 * 25 µG

UOM: 1 * 25 µG

Promotion

Numéro de catalogue: (STMC100-0720)

Fournisseur: STEMCELL Technologies

Description: Animal origin-free suspension culture medium for human ES and iPS cells.

UOM: 1 * 1 KIT

Promotion

 Il s'agit d'un élément MarketSource. Des frais supplémentaires peuvent s'appliquer.

Numéro de catalogue: (SOCO521.592)

Fournisseur: Socorex Isba

Description: [EN]GUIDE BAR FIXING PLATE 50ML SOCO 1 * 1 Pce

UOM: 1 * 1 ST

Promotion

Numéro de catalogue: (BOSSBS-8225R-A750)

Fournisseur: Bioss

Description: FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.

UOM: 1 * 100 µl

Promotion

Numéro de catalogue: (BOSSBS-4708R-A680)

Fournisseur: Bioss

Description: Alpha 1 Fetoprotein is a major plasma protein produced by the yolk sac and the liver during foetal life. Alpha fetoprotein expression in adults is often associated with hepatoma or teratoma. However, hereditary persistance of alpha-fetoprotein may also be found in individuals with no obvious pathology. The protein is thought to be the foetal counterpart of serum albumin, and the alpha fetoprotein and albumin genes are present in tandem in the same transcriptional orientation on chromosome 4. Alpha fetoprotein is found in monomeric as well as dimeric and trimeric forms, and binds copper, nickel, fatty acids and bilirubin. The level of alpha fetoprotein in amniotic fluid is used to measure renal loss of protein to screen for spina bifida and anencephaly. Expression has been documented in human adrenal, liver, ovary, testis, and pancreas. ESTs have been isolated from normal human brain, liver/spleen, embryo and uterus tissue libraries.

UOM: 1 * 100 µl

Promotion

Numéro de catalogue: (BOSSBS-11903R-A680)

Fournisseur: Bioss

Description: Nur77 (also designated NGFI-B), Nurr1 (Nur-related factor 1), and NOR-1 (neuron-derived orphan receptor 1) constitute the NGFI-B subfamily within the nuclear receptor superfamily. Ligands for these protein have not been identified, and, therefore, they are designated orphan nuclear receptors. Genes of the NGFI-B subfamily are classified as immediate-early genes, which are induced rapidly, but transiently, in response to a variety of stimuli. They have been implicated in cell proliferation, differentiation, and apoptosis. The human NOR-1 gene maps to chromosome 9q, and encodes a protein which is expressed in heart, skeletal muscle, thymus, and spleen as well as in brain, where it is developmentally regulated. There-fore, NOR-1 may be involved in regulating neural differentiation. The NOR-1 gene also undergoes chromosomal translocation with the EWS gene to produce a protein thought to affect pre-mRNA splicing.

UOM: 1 * 100 µl

Promotion

Numéro de catalogue: (BOSSBS-8225R-A680)

Fournisseur: Bioss

Description: FAM168A is a 244 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11, which makes up around 4% of human genomic DNA and is considered a gene and disease association dense chromosome. The chromosome 11 encoded Atm gene is important for regulation of cell cycle arrest and apoptosis following double strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. The blood disorders Sickle cell anemia and thalassemia are caused by HBB gene mutations. Wilms' tumors, WAGR syndrome and Denys-Drash syndrome are associated with mutations of the WT1 gene. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are also associated with defects in chromosome 11.

UOM: 1 * 100 µl

Promotion