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1-Methylpiperazin-2-one+hydrochloride
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1-Methylpiperazin-2-one+hydrochloride
Catalog Number:
(10298-112)
Supplier:
Bioss
Description:
GLYATL1 is a 302 amino acid mitochondrial acyltransferase that transfers the acyl group to the N-terminus of glycine. GLYATL1 can also conjugate a multitude of substrates to form a variety of N-acylglycines. A member of the glycine N-acyltransferase family, GLYATL1 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q12.1. Chromosome 11 houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
Supplier:
TCI America
Description:
CAS Number: 40470-68-6
Molecular Formula: C30H26O2 Molecular Weight: 418.54 Purity/Analysis Method: >90.0% (HPLC) Form: Crystal Melting point (°C): 218
Supplier:
BeanTown Chemical
Description:
CAS: 600-00-0; EC No: 209-980-6; MDL No: MFCD00000123
UN No: UN2924; Haz Class: 3(8); Packing Group: III
Liquid; Linear Formula: (CH3)2CBrCOOCH2CH3; Molecular Formula: C6H11BrO2; MW: 195.06
Boiling Point: 65-67°/11 mmHg; Flash point: 60°C (140°F)
Density (g/mL): 1.329; Refractive Index: 1.444
Supplier:
Sino Biological
Description:
A DNA sequence encoding the mouse Il11 (NP_032376.1) (Pro22-Leu199) was expressed.
Catalog Number:
(10477-550)
Supplier:
Bioss
Description:
HkRP3, also known as CCDC88B (coiled-coil domain-containing protein 88B) or BRLZ (brain leucine zipper domain-containing protein), is a 1,476 amino acid protein that belongs to the CCDC88 family. Members of the hook-related protein family are characterized by the presence of a C-terminal hook-related domain and an N-terminal potential microtubule binding domain. HkRP3 may be involved in the linkage of various organelles to microtubules, and exists as six alternatively spliced isoforms. The gene encoding HkRP3 maps to human chromosome 11q13.1 and mouse chromosome 19 A. Chromosome 11 houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
Catalog Number:
(10265-748)
Supplier:
Bioss
Description:
MPPED2 (Metallophosphoesterase domain-containing protein 2), also known as C11orf8, FAM1B or 239FB, is a 294 amino acid protein. Expressed primarily in fetal brain tissue, MPPED2 is encoded by a gene that maps to chromosome 11. With approximately 135 million base pairs and 1,400 genes, chromosome 11 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 stranded 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, while 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.
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 007484-1G , MDL Number: MFCD03426089
Supplier:
AMBEED, INC
Description:
4,4'-Bis(bromomethyl)biphenyl 95%
Supplier:
Hichrom
Description:
Avantor® ACE® UltraCore Biphenyl are high performing solid-core (core-shell) particle columns, designed for a range of chromatographic applications and is especially well suited for retention of aromatic compounds that elute early on alkyl phases.
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
(S)-N-Boc-α-ethylalanine 98%, 98% ee
Catalog Number:
(10298-132)
Supplier:
Bioss
Description:
GLYATL1 is a 302 amino acid mitochondrial acyltransferase that transfers the acyl group to the N-terminus of glycine. GLYATL1 can also conjugate a multitude of substrates to form a variety of N-acylglycines. A member of the glycine N-acyltransferase family, GLYATL1 exists as two alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q12.1. Chromosome 11 houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
Catalog Number:
(102520-212)
Supplier:
Matrix Scientific
Description:
MF=C13H9F3 MW=222.21 CAS=362-59-4 MDL=MFCD14525536 1G
Catalog Number:
(102892-686)
Catalog Number:
(10072-876)
Supplier:
Prosci
Description:
CT-1 is a member of the IL-6 family of cytokines which also includes LIF, CNTF, OSM (Oncostatin M), IL-11, IL-6 and possibly NT-1/ BSF-3. CT-1 is a pleiotropic cytokine which is expressed in various tissues including the adult heart, skeletal muscle, ovary, colon, prostate and fetal lung and signals through the LIF receptor and the gp130 receptor subunit. CT-1 has the ability to induce cardiac myocyte hypertrophy, and enhances the survival of cardiomyocyte and different neuronal populations. Biologically active human CT-1 is synthesized as a 201 amino acid polypeptide lacking a hydrophobic N-terminal secretion signal sequence. Recombinant Human CT-1 is a 21.5 kDa protein consisting of 201 amino acid residues.
Catalog Number:
(103633-286)
Supplier:
Sino Biological
Description:
A DNA sequence encoding the Influenza A virus (A/duck/Eastern China/11/2009(H6N6)) hemagglutinin (AEF59343.1) (Met1-Arg344), termed as HA1, was expressed with a polyhistidine tag at the C-terminus.
Catalog Number:
(76108-260)
Supplier:
Bioss
Description:
The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion, and drug extrusion and delivery. CCDC83 (coiled-coil domain-containing protein 83), also known as HSD9, is 413 amino acid protein that exists as three alternatively spliced isoforms. The gene encoding CCDC83 maps to human chromosome 11, which houses over 1,400 genes and comprises nearly 4% of the human genome. Jervell and Lange-Nielsen syndrome, Jacobsen syndrome, Niemann-Pick disease, hereditary angioedema and Smith-Lemli-Opitz syndrome are associated with defects in genes that maps to chromosome 11.
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the
is still displayed and you need assistance, please call us at 1-800-932-5000.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at Regulatory_Affairs@vwr.com
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