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Ethyl+isothiocyanatoformate
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Ethyl+isothiocyanatoformate
Supplier:
TCI America
Description:
CAS Number: 20306-22-3
MDL Number: MFCD00050452 Molecular Formula: C14H20O4 Molecular Weight: 252.31 Purity/Analysis Method: >98.0% (GC) Form: Clear Liquid Specific Gravity (20/20): 1.06
Supplier:
Strem Chemicals Inc
Description:
Metallocenes, Derivatives & Cp Precursors
Catalog Number:
(76692-586)
Supplier:
AMBEED, INC
Description:
2-Hydroxy-4-methylbenzamide 95%
Catalog Number:
(10311-090)
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. Translo-acations 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. The C22orf26 gene product has been provisionally designated C22orf26 pending further characterization.
Supplier:
AMBEED, INC
Description:
Ethyl 2-(6-chloropyridin-2-yl)acetate, Purity: 97%, CAS Number: 174666-22-9, Appearance: Colorless or White to Yellow Solid or liquid, Storage: Inert atmosphere, 2-8C, Size: 100MG
Catalog Number:
(10664-262)
Supplier:
Bioss
Description:
Neuronal axonal membrane protein Nap-22, also designated neuronal tissue-enriched acidic protein or brain acid soluble protein (BASP1), is a Ca2+-dependent calmodulin-binding protein that is important for neuronal sprouting and plasticity. Nap-22 is abundant in brain nerve terminals and is also present in significant amounts in kidney, testis and lymphoid tissue. Nap-22 undergoes N-terminal myristoylation for membrane localization. It has been characterized as a major protein of neuronal rafts, which are known to preferentially bind membranes containing cholesterol. Nap-22 is a crucial protein active in neurite outgrowth and synaptic plasticity.
Catalog Number:
(10664-268)
Supplier:
Bioss
Description:
Neuronal axonal membrane protein Nap-22, also designated neuronal tissue-enriched acidic protein or brain acid soluble protein (BASP1), is a Ca2+-dependent calmodulin-binding protein that is important for neuronal sprouting and plasticity. Nap-22 is abundant in brain nerve terminals and is also present in significant amounts in kidney, testis and lymphoid tissue. Nap-22 undergoes N-terminal myristoylation for membrane localization. It has been characterized as a major protein of neuronal rafts, which are known to preferentially bind membranes containing cholesterol. Nap-22 is a crucial protein active in neurite outgrowth and synaptic plasticity.
Supplier:
Strem Chemicals Inc
Description:
CAS #: 7440-22-4. Size: 100square centimeters.
Supplier:
AMBEED, INC
Description:
2-Amino-3,5-dimethylbenzenesulfonic acid, Purity: 98%, CAS Number: 88-22-2, Appearance: White to light yellow powder to crystal, Storage: Keep in dark place, Inert atmosphere, Room temperature, Size: 5g
Supplier:
AMBEED, INC
Description:
4-Fluoro-2-(trifluoromethyl)aniline 98%
Supplier:
AMBEED, INC
Description:
((3aR,4R,6R,6aR)-6-Methoxy-2,2-dimethyltetrahydrofuro[3,4-d][1,3]dioxol-4-yl)methanol, Purity: 95%, CAS Number: 4099-85-8, Appearance: Colorless to Yellow Liquid, Storage: Inert atmosphere, 2-8C, Size: 250MG
Catalog Number:
(10476-324)
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:
Matrix Scientific
Description:
2-Anilinoquinolin-8-ol
Supplier:
AMBEED, INC
Description:
5-(Trifluoromethoxy)picolinonitrile 95%
Supplier:
AMBEED, INC
Description:
2-Aminoquinoline 97%
Catalog Number:
(10666-566)
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.
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is still displayed and you need assistance, please call us at 1-800-932-5000.
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