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You Searched For:

(S)-(+)-2,2-Dimethylcyclopropanecarboxylic+acid


141,792  results were found

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Supplier:  AMBEED, INC
Description:   6-Oxo-piperidine-2-carboxylic acid ≥95%
New Product
Supplier:  Bioss
Description:   C22orf9 is a 404 amino acid protein that exists as three alternatively spliced isoforms and is encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chromosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.
Supplier:  ALADDIN SCIENTIFIC
Description:   4-Amino-3-(trifluoromethoxy)benzoic acid ≥98%
New Product
Supplier:  Bachem Americas
Description:   Sequence: Boc-Arg(Pbf)-OH
Supplier:  TCI America
Description:   CAS Number: 1670-82-2
MDL Number: MFCD00210441
Molecular Formula: C9H7NO2
Molecular Weight: 161.16
Purity/Analysis Method: >98.0% (HPLC,T)
Form: Crystal
Melting point (°C): 257
MSDS SDS

Supplier:  Bioss
Description:   C22orf31, also known as HS747E2A or bK747E2.1, is a 290 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.

Supplier:  Bioss
Description:   Chromosome 22 contains over 500 genes and about 49 million bases. Being the second smallest human chromosome, 22 contains a surprising variety of interesting genes. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia. CCDC134 (coiled-coil domain containing 134), also known as MGC21013 or FLJ22349, is a 229 amino acid protein encoded by a gene mapping to human chromosome 22.

Supplier:  Rockland Immunochemical
Description:   This product has been assayed against 1.0 µg of Rabbit IgG in a standard capture ELISA using Peroxidase Conjugated Streptavidin and ABTS (2,2’-azino-bis-[3-ethylbenthiazoline-6-sulfonic acid])
MSDS SDS
Supplier:  Labconco
Description:   Safely store and vent acids and other highly corrosive liquids.
Product available on GSA Advantage®

Supplier:  Matrix Scientific
Description:   1-(1-Methylbutyl)-5-oxopyrrolidine-3-carboxylic acid
Supplier:  Rockland Immunochemical
Description:   Anti-Mutarotase has been assayed against 1.0 µg of Mutarotase (Porcine Kidney) in a standard capture ELISA using ABTS (2,2’-azino-bis-[3-ethylbenthiazoline-6-sulfonic acid])
Supplier:  Bioss
Description:   C22orf31, also known as HS747E2A or bK747E2.1, is a 290 amino acid protein encoded by a gene located on human chromosome 22, which contains over 500 genes and about 49 million bases. As the second smallest human chromosome, chomosome 22 contains a wide variety of genes with numerous functions. Phelan-McDermid syndrome, Neurofibromatosis type 2 and autism are associated with chromosome 22. A schizophrenia susceptibility locus has been identified on chromosome 22 and studies show that 22q11 deletion symptoms include a high incidence of schizophrenia. Translocations between chromosomes 9 and 22 may lead to the formation of the Philadelphia Chromosome and the subsequent production of the novel fusion protein, BCR-Abl, a potent cell proliferation activator found in several types of leukemia.
Supplier:  Matrix Scientific
Description:   MF=C23H44N2O6 MW=444.62 CAS=560088-79-1 MDL=MFCD06796877 5G

Supplier:  Rockland Immunochemical
Description:   Anti-Mouse IgG F(c) Antibody has been assayed against 1.0 µg of Mouse IgG in a standard capture ELISA using Peroxidase Conjugated Streptavidin and ABTS (2,2’-azino-bis-[3-ethylbenthiazoline-6-sulfonic acid])

Supplier:  Rockland Immunochemical
Description:   This product has been assayed against 1.0 µg of Human IgA in a standard capture ELISA using Peroxidase Conjugated Streptavidin and ABTS (2,2’-azino-bis-[3-ethylbenthiazoline-6-sulfonic acid])
Catalog Number: (TCI0358-005G)

Supplier:  TCI America
Description:   CAS Number: 17046-22-9
MDL Number: MFCD00041743
Molecular Formula: C7H11NO3
Molecular Weight: 157.17
Purity/Analysis Method: >95.0% (GC)
Form: Clear Liquid
Boiling point (°C): 79
Flash Point (°C): 88
Specific Gravity (20/20): 1.06
MSDS SDS
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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 at 1-800-932-5000.
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 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
-Additional Documentation May be needed to purchase this item. A VWR representative will contact you if needed.
This product has been blocked by your organization. Please contact your purchasing department for more information.
The original product is no longer available. The replacement shown is available.
This product is no longer available. Alternatives may be available by searching with the VWR Catalog Number listed above. If you need further assistance, please call VWR Customer Service at 1-800-932-5000.
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