(S)-(+)-2,2-Dimethylcyclopropanecarboxylic+acid
Catalog Number:
(77686-538)
Supplier:
AMBEED, INC
Description:
6-Oxo-piperidine-2-carboxylic acid ≥95%
Catalog Number:
(76121-134)
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%
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
Catalog Number:
(10666-568)
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.
Catalog Number:
(10476-322)
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.
Catalog Number:
(RL611-1604)
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])
Supplier:
Labconco
Description:
Safely store and vent acids and other highly corrosive liquids.
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Catalog Number:
(102668-456)
Supplier:
Matrix Scientific
Description:
1-(1-Methylbutyl)-5-oxopyrrolidine-3-carboxylic acid
Catalog Number:
(RL200-4362S)
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])
Catalog Number:
(10666-576)
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
Catalog Number:
(RL610-1603)
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])
Catalog Number:
(RL609-4606)
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
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