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N-Carbobenzoxy-L-proline ≥98%

Supplier: Thermo Fisher Scientific
Description: N-Carbobenzoxy-L-proline ≥98%

MSDS

Product Image-ACRO406415000

4,4'-Diaminostilbene-2,2'-disulphonic Acid 95%

Supplier: Thermo Fisher Scientific
Description: Appearance: Cream to yellow-brown Crystalline powder

MSDS

Product Image-K940-100ML

Trypan blue 4 g/l in aqueous solution cell culture reagent

Catalog Number: (K940-100ML)
Supplier: VWR Chemicals
Description: A pre-mixed dye solution used in cell culture applications to determine cell viability. A researcher can remove a sample of cells from culture and combine in a 1:1 ratio with the Trypan Blue solution. Under the microscope, dead cells will appear a blue color and viable cells will appear clear and translucent. Using a hemacytometer (gridded microscope slide), a researcher can quantify the percentage of dead cells within a population. Stained cells are ready for counting within five minutes.
UOM: 1 * 100 mL

MSDS Certificates


Image Unavailable-APOSOR911785-100G

Ethyl 2,3-Dicyanopropionate 95%

Supplier: Apollo Scientific
Description: Ethyl 2,3-Dicyanopropionate 95%

Image Unavailable-APOSPC5843-1G

Perfluoro-2,5,8,11,14-pentamethyl-3,6,9,12,15-pentaoxaoctadecanoyl fluoride 90+%

Supplier: Apollo Scientific
Description: Typically 92%, bal. other HFPO oligomer acid fluorides

Product Image-ACRO396780050

Methyl-4-(aminomethyl)benzoate hydrochloride 97%

Supplier: Thermo Fisher Scientific
Description: Methyl-4-(aminomethyl)benzoate hydrochloride 97%

MSDS

Image Unavailable-BOSSBS-8409R-A680

Anti-GLB1L3 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Catalog Number: (BOSSBS-8409R-A680)
Supplier: Bioss
Description: GLB1L3 is a 653 amino acid protein belonging to the glycosyl hydrolase 35 family. GLB1L3 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q25. 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 strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. 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
Image Unavailable-BOSSBS-8409R-A488

Anti-GLB1L3 Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Catalog Number: (BOSSBS-8409R-A488)
Supplier: Bioss
Description: GLB1L3 is a 653 amino acid protein belonging to the glycosyl hydrolase 35 family. GLB1L3 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q25. 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 strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. 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
Image Unavailable-BOSSBS-8409R-CY5.5

Anti-GLB1L3 Rabbit Polyclonal Antibody (Cy5.5®)

Catalog Number: (BOSSBS-8409R-CY5.5)
Supplier: Bioss
Description: GLB1L3 is a 653 amino acid protein belonging to the glycosyl hydrolase 35 family. GLB1L3 exists as three alternatively spliced isoforms and is encoded by a gene that maps to human chromosome 11q25. 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 strand DNA breaks. Atm mutation leads to the disorder known as ataxia-telangiectasia. 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
Image Unavailable-ENZOBMLEI2660005

MK-886 ≥98% (by HPLC)

Supplier: ENZO LIFE SCIENCES
Description: Inhibitor of PPARα activation. Inhibits 5-lipoxygenase-activating protein (FLAP) and leukotriene biosynthesis. Binds to FLAP with high affinity and prevents the activation of 5-lipoxygenase. IC50’s for leukotriene biosynthesis: 2.5 nM in intact leukocytes; 1.1 µM in whole blood. Induces apoptosis through the mitochondrial pathway.

Image Unavailable-APOSOR40702-5G

tert-Butyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate 98%

Supplier: Apollo Scientific
Description: tert-Butyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-5,6-dihydropyridine-1(2H)-carboxylate 98%

Product Image-87873.180

Eriochrome Black T 1% in sodium chloride Reag. Ph. Eur. 1056801

Catalog Number: (87873.180)
Supplier: VWR Chemicals
Description: Eriochrome Black T 1% in sodium chloride Reag. Ph. Eur. 1056801
UOM: 1 * 100 g

MSDS Certificates


Product Image-ENZOBMLFA0090100

all cis-8,11,14-Eicosatrienoic acid ≥99% (by GC), clear liquid, Ultrapure

Supplier: ENZO LIFE SCIENCES
Description: Beneficial effects in cardiovascular diseases and inflammation.

Image Unavailable-ENZOBMLPI1430010

Nafamostat mesylate ≥98%

Supplier: ENZO LIFE SCIENCES
Description: Tryptase inhibitor

Image Unavailable-BOSSBS-11607R-A750

Anti-TSK/Tsukushin/LRRC54 Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (BOSSBS-11607R-A750)
Supplier: Bioss
Description: The leucine-rich (LRR) repeat is a 20 to 30 amino acid motif that forms a hydrophobic / horseshoe fold, allowing it to accommodate several leucine residues within a tightly packed core. All LRR repeats contain a variable segment and a highly conserved segment, the latter of which accounts for 11 or 12 residues of the entire LRR motif. LRRC54 (leucine-rich repeat-containing protein 54), also known as tsukushin, TSKU or E2-induced gene 4 protein (E2IG4), is a 353 amino acid secreted protein that likely localizes to the cell membrane and extracellular compartments. Involved in extracellular secretion and intracellular transport, LRRC54 can be induced by 17-beta-estradiol. Containing nine LRR repeat and a cleavable signal peptide, the gene encoding LRRC54 maps to human chromosome 11, which houses over 1400 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.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-9635R-CY3

Anti-SLC39A11 Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (BOSSBS-9635R-CY3)
Supplier: Bioss
Description: Zinc is an essential cofactor that is involved in cell growth and development, as well as in protein, nucleic acid and lipid metabolism. The transport of zinc across the cell membrane is crucial for correct enzyme and overall cell function. SLC39A11 (solute carrier family 39 (metal ion transporter), member 11), also known as ZIP11 (Zrt- and Irt-like protein 11), is a 342 amino acid multi-pass membrane protein belonging to the ZIP transporter family. Expressed as multiple alternatively spliced isoforms, SLC39A11 acts as a zinc-influx transporter and is encoded by a gene located on human chromosome 17, which comprises over 2.5% of the human genome and encodes over 1,200 genes, some of which are involved in tumor suppression and in the pathogenesis of Li-Fraumeni syndrome, early onset breast cancer and a predisposition to cancers of the ovary, colon, prostate gland and fallopian tubes.
UOM: 1 * 100 µl
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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 call is still displayed and you need assistance, please call us on +353 1 88 22222.
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 eurega_services@eu.vwr.com
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The original product is no longer available. The replacement shown is available.
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