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You Searched For: Benzo[b]thiophene-2-carboxylic+acid


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Product Image-KAVA632414321940

Laboratory bottles, narrow neck, with screw cap

Description: Borosilicate glass 3,3, clear or brown.
Catalog Number: KAVA632414321940
UOM: 1 * 10 items
Supplier: Kavalier
Product Image-KING060205/9500086

Sponges, Spontex®

Description: These sponges are made from 100% natural and cellulose.
Catalog Number: KING060205/9500086
UOM: 1 * 1 items
Supplier: KING DISPOSABLES
Product Image-214-1343

Flasks acc. to Kjeldahl

Description: Borosilicate glass 3.3.
Catalog Number: 214-1343
UOM: 1 * 1 items
Supplier: Kavalier
Image Unavailable-13152-6X2.5KG

Magnesium chloride hexahydrate 99-101%, Puriss., meets analytical specification of BP, FCC, Ph. Eur., E511 (max. 0.0001% Al), Fluka™

Description: Magnesium chloride hexahydrate 99-101%, Puriss., meets analytical specification of BP, FCC, Ph. Eur., E511 (max. 0.0001% Al), Fluka™
Catalog Number: 13152-6X2.5KG
UOM: 1 * 15 kg
Supplier: Honeywell Chemicals

MSDS


Image Unavailable-BOSSBS-9498R-A680

Anti-C9orf153 Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Description: C9orf153 is a 101 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf153 maps to human chromosome 9q21.33. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterised by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukaemias.
Catalog Number: BOSSBS-9498R-A680
UOM: 1 * 100 µl
Supplier: Bioss
Product Image-HACH42453

Buffer solutions for hardness testing

Description: This buffer is used for hardness and chelant determination by titration.
Catalog Number: HACH42453
UOM: 1 * 1 L
Supplier: Hach
Image Unavailable-MOLEM23320388

4-(Phenylazo)diphenylamine

Description: 4-(Phenylazo)diphenylamine
Catalog Number: MOLEM23320388
UOM: 1 * 25 g
Supplier: Molekula
Product Image-80.625

Transport swabs

Description: Transport swabs are neutral which is for use on intact skin and in natural body openings.
Catalog Number: 80.625
UOM: 1 * 500 items
Supplier: SARSTEDT
Image Unavailable-BOSSBS-9498R-A350

Anti-C9ORF153 Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Description: C9orf153 is a 101 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf153 maps to human chromosome 9q21.33. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Catalog Number: BOSSBS-9498R-A350
UOM: 1 * 100 µl
Supplier: Bioss
Image Unavailable-BOSSBS-12020R-HRP

Anti-GPR101 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))

Description: G protein-coupled receptors (GPRs), also known as seven transmembrane receptors, heptahelical receptors or 7TM receptors, comprise a superfamily of proteins that play a role in many different stimulus-response pathways. G protein coupled receptors translate extracellular signals into intracellular signals (G protein activation) and they respond to a variety of signaling molecules, such as hormones and neurotransmitters. GPR101 (G protein-coupled receptor 101), also known as GPCR6, is a 508 amino acid multi-pass membrane protein that belongs to the G-protein coupled receptor 1 family. GPR101 functions as an orphan receptor that is thought to play a role in signaling events throughout the cell. Expressed predominantly in brain, GPR101 participates in a wide range of activities in the CNS via modulation of cAMP levels.
Catalog Number: BOSSBS-12020R-HRP
UOM: 1 * 100 µl
Supplier: Bioss
Product Image-212-6894

Test tubes, with rim

Description: PS or PP.
Catalog Number: 212-6894
UOM: 1 * 2.000 items
Supplier: KARTELL
Product Image-548-2194

Closures for 13 mm screw neck vials, Chromacol™

Description: PP screw caps with or without seals.
Catalog Number: 548-2194
UOM: 1 * 500 items
Supplier: CHROMACOL
Product Image-GOSSPR800-01

Jars, wide mouth, with screw cap, Corning® Gosselin™

Description: PP, white.
Catalog Number: GOSSPR800-01
UOM: 1 * 100 items
Supplier: Corning

Environmentally Preferable


Product Image-GAINEF1F-083OR

DYMO-Compatible Cryogenic Labels

Description: DYMO compatible direct thermal cryo labels with permanent adhesive.
Catalog Number: GAINEF1F-083OR
UOM: 1 * 1 Roll
Supplier: GA
Product Image-215-9004

Bottles, wide neck, square, with screw cap

Description: HDPE, translucent.
Catalog Number: 215-9004
UOM: 1 * 1 items
Supplier: LAMAPLAST
Image Unavailable-BOSSBS-9498R-FITC

Anti-C9ORF153 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Description: C9orf153 is a 101 amino acid protein that exists as two alternatively spliced isoforms. The gene encoding C9orf153 maps to human chromosome 9q21.33. Chromosome 9 consists of about 145 million bases, represents 4% of the human genome and encodes nearly 900 genes. Thought to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, is associated with the chromosome 9 gene encoding endoglin protein, ENG. Familial dysautonomia is also associated with chromosome 9 though through the gene IKBKAP. Notably, chromosome 9 encompasses the largest interferon family gene cluster. Chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Catalog Number: BOSSBS-9498R-FITC
UOM: 1 * 100 µl
Supplier: Bioss
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