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Numéro de catalogue: (PRSI25-112)
Fournisseur: ProSci Inc.
Description: PML is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. PML localizes to nuclear bodies where it functions as a transcription factor and tumor suppressor. Its expression is cell-cycle related and it regulates the p53 response to oncogenic signals. The gene is often involved in the translocation with the retinoic acid receptor alpha gene associated with acute promyelocytic leukemia (APL). Extensive alternative splicing of this gene results in several variations of the protein's central and C-terminal regions; all variants encode the same N-terminus.
UOM: 1 * 50 µG


Numéro de catalogue: (PRSI56-968)
Fournisseur: ProSci Inc.
Description: The protein encoded by this gene is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. This protein localizes to the nucleus and the cytoplasm. Its function has not been identified. [provided by RefSeq].
UOM: 1 * 400 µl

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Fournisseur: Thermo Fisher Scientific
Description: 1,3,5-Trichlorobenzène ≥98%
Fournisseur: TCI
Description: 1,3,5-Tris(4-formylphenyl)benzene ≥96.0% (par HPLC)

Fournisseur: Thermo Fisher Scientific
Description: 1,3,5-Triphénylbenzène ≥99%
Fournisseur: Apollo Scientific
Description: (1,3,5-Trimethyl-1H-pyrazol-4-yl)methylamine 97%

Numéro de catalogue: (APOSOR8150-1G)
Fournisseur: Apollo Scientific
Description: 1,3,5-Trimethyl-1H-pyrazole-4-sulphonylchloride 97%
UOM: 1 * 1 g


Numéro de catalogue: (BOSSBS-9380R-HRP)
Fournisseur: Bioss
Description: Midline-1 (Tripartite motif-containing protein 18, Putative transcription factor XPRF, RING finger protein 59) is a 667 amino acid protein encoded by the human gene MID1. Midline-1 belongs to the TRIM/RBCC family and contains two B box-type zinc fingers, one B30.2/SPRY domain, one COS domain, one fibronectin type-III domain and one RING-type zinc finger. Midline-1 is believed to have E3 ubiquitin ligase activity which targets the catalytic subunit of protein phosphatase 2 for degradation. It is a cytoplasmic protein found as a homodimer or heterodimer with Midline-2. It also interacts with IGBP1 (Lymphocyte signaling protein A4). Defects in MID1 are the cause of Opitz syndrome type I (OS-I). OS-I is an X-linked recessive disorder characterized by hypertelorism, genital-urinary defects such as hypospadias in males and splayed labia in females, lip-palate-laryngotracheal clefts, imperforate anus, developmental delay and congenital heart defects. OS-I mutations produce proteins with a decreased affinity for microtubules.
UOM: 1 * 100 µl


Numéro de catalogue: (BOSSBS-9380R-A350)
Fournisseur: Bioss
Description: Midline-1 (Tripartite motif-containing protein 18, Putative transcription factor XPRF, RING finger protein 59) is a 667 amino acid protein encoded by the human gene MID1. Midline-1 belongs to the TRIM/RBCC family and contains two B box-type zinc fingers, one B30.2/SPRY domain, one COS domain, one fibronectin type-III domain and one RING-type zinc finger. Midline-1 is believed to have E3 ubiquitin ligase activity which targets the catalytic subunit of protein phosphatase 2 for degradation. It is a cytoplasmic protein found as a homodimer or heterodimer with Midline-2. It also interacts with IGBP1 (Lymphocyte signaling protein A4). Defects in MID1 are the cause of Opitz syndrome type I (OS-I). OS-I is an X-linked recessive disorder characterized by hypertelorism, genital-urinary defects such as hypospadias in males and splayed labia in females, lip-palate-laryngotracheal clefts, imperforate anus, developmental delay and congenital heart defects. OS-I mutations produce proteins with a decreased affinity for microtubules.
UOM: 1 * 100 µl


Numéro de catalogue: (BOSSBS-9238R-CY5)
Fournisseur: Bioss
Description: The RING-type zinc finger motif is present in a number of viral and eukaryotic proteins and is made of a conserved cysteine-rich domain that is able to bind two zinc atoms. Proteins that contain this conserved domain are generally involved in the ubiquitination pathway of protein degradation. RNF23 (RING finger protein 23), also known as tripartite motif-containing protein 39 (TRIM39) or testis-abundant finger protein, is a 518 amino acid protein belonging to the TRIM/RBCC family that is known to interact with MOAP1. Ubiquitously expressed and existing as two alternatively spliced isoforms, RNF23 is found at highest levels in spleen, testis, brain, kidney, liver, heart and skeletal muscle. RNF23 typically localizes to cytosol but shifts to mitochondria upon co-localization with MOAP1, a short-lived, pro-apoptotic protein which RNF23 prevents from becoming poly-ubiquitinated and degraded, thereby facilitating apoptosis. RNF23 contains one B box-type zinc finger, a B30.2/SPRY domain and a single RING-type zinc finger.
UOM: 1 * 100 µl


Numéro de catalogue: (APOSOR27312-1G)
Fournisseur: Apollo Scientific
Description: 4-(Methylthio)-6-(2-thienyl)-1,3,5-triazin-2-amine
UOM: 1 * 1 g


Numéro de catalogue: (APOSOR46644-1G)
Fournisseur: Apollo Scientific
Description: 1-Bicyclo[4.2.0]octa-1,3,5-trien-7-ylmethanamine
UOM: 1 * 1 g


Fournisseur: Apollo Scientific
Description: 4-Cyclopropyl-6-(methylthio)-1,3,5-triazin-2-amine

Numéro de catalogue: (APOSOR110409-1G)
Fournisseur: Apollo Scientific
Description: 1,3,5-Trimethyl-1H-pyrazole-4-carbonyl chloride
UOM: 1 * 1 g


Numéro de catalogue: (APOSOR23237-5G)
Fournisseur: Apollo Scientific
Description: 1,3,5-Trimethyl-1H-pyrazole-4-carbaldehyde 97%
UOM: 1 * 5 g


Numéro de catalogue: (PRSI28-121)
Fournisseur: ProSci Inc.
Description: TRIM17 encodes a protein that is a member of the tripartite motif (TRIM) family. The TRIM motif includes three zinc-binding domains, a RING, a B-box type 1 and a B-box type 2, and a coiled-coil region. The protein localizes to cytoplasmic bodies. The protein is expressed at high levels in the testis, but its function is unknown.
UOM: 1 * 50 µG


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