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2,2\\\'-Dithiodi(benzoic+acid)
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2,2\\\'-Dithiodi(benzoic+acid)
Supplier:
Shenandoah Biotechnology
Description:
Fibroblast growth factor 22 (FGF-22) is a mediator of synaptogenesis in the adult nervous system and functions to regulate synapse formation and maturation. FGF-22 is expressed in the inner hair cell and functions to maintain ribbon synapse number to protect functional hearing. In the hippocampus, FGF-22 promotes excitatory synapse formation through binding the FGFR2b and FGFR1b receptors. FGF-22 is also required for axonal circuit remodeling after spinal cord injury.
Catalog Number:
(TS22881-2500)
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
γ-L-Glutamyl-L-Glutamic Acid
Catalog Number:
(10448-210)
Supplier:
Bioss
Description:
CESK1, also known as CCT8L2 (chaperonin containing TCP1, subunit 8 theta-like 2), is a 557 amino acid protein that localizes to the cytoplasm and is thought to function as a molecular chaperone, possibly assisting protein folding after ATP hydrolysis. CESK1 belongs to the TCP-1 chaperonin family and is encoded by a gene which maps to human chromosome 22. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, neurofibromatosis type 2, autism and schizophrenia. Additionally, 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 leukemias.
Catalog Number:
(EM1.02315.0005)
Catalog Number:
(10481-638)
Supplier:
Bioss
Description:
ANKRD54 is a 300 amino acid protein that contains four ankyrin repeats and is expressed as two alternatively spliced isoforms. The gene encoding human ANKRD54 maps to chromosome 22, which houses over 500 genes and is the second smallest human chromosome. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, neurofibromatosis type 2, autism and schizophrenia. Additionally, 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 leukemias.
Supplier:
AMBEED, INC
Description:
Ethyl 2-Cyano-2-methylpropionate, Purity: 98%, CAS Number: 1572-98-1, Appearance: Liquid, Storage: Sealed in dry, Room Temperature, Size: 500g
Catalog Number:
(101850-032)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 040715-500MG , MDL Number: MFCD06010034
Supplier:
TCI America
Description:
(stabilized with MEHQ)
CAS Number: 693-38-9 MDL Number: MFCD00059288 Molecular Formula: C18H34O2 Molecular Weight: 282.47 Purity/Analysis Method: >96.0% (GC) Form: Crystal Flash Point (°C): 176 Freezing point (°C): 22
Catalog Number:
(101836-074)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 033639-500MG , MDL Number: MFCD05844466
Supplier:
TCI America
Description:
CAS Number: 141-04-8
MDL Number: MFCD00053722 Molecular Formula: C14H26O4 Molecular Weight: 258.36 Purity/Analysis Method: >99.0% (GC) Form: Clear Liquid Boiling point (°C): 293 Flash Point (°C): 156 Freezing point (°C): -22 Specific Gravity (20/20): 0.95
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
Glyoxylic acid monohydrate 98%, pure
Catalog Number:
(10446-552)
Supplier:
Bioss
Description:
CESK1, also known as CCT8L2 (chaperonin containing TCP1, subunit 8 theta-like 2), is a 557 amino acid protein that localizes to the cytoplasm and is thought to function as a molecular chaperone, possibly assisting protein folding after ATP hydrolysis. CESK1 belongs to the TCP-1 chaperonin family and is encoded by a gene which maps to human chromosome 22. Mutations in several of the genes that map to chromosome 22 are involved in the development of Phelan-McDermid syndrome, neurofibromatosis type 2, autism and schizophrenia. Additionally, 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 leukemias.
Catalog Number:
(101834-970)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 033080-500MG , MDL Number: MFCD03420242
Supplier:
AMBEED, INC
Description:
5-Methyl-1H-pyrazole-3-carboxylic acid 97%
Catalog Number:
(76110-536)
Supplier:
Bioss
Description:
ODF3B, also known as ODF3L3 (outer dense fiber protein 3-like protein 3), is a 253 amino acid protein belonging to the ODF3 family. Existing as two isoforms produced by alternative splicing, ODF3B contains one DUF1309 repeat. The gene that encodes ODF3B maps to human chromosome 22, which 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.
Supplier:
MP Biomedicals
Description:
L-Tryptophan is an amino acid precursor of serotonin and melatonin.
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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
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
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