(2S,2'S)-2,2'-(Hexadecanedioylbis(azanediyl))dipentanedioic+acid
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.
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:
(76483-132)
Supplier:
AAT BIOQUEST INC
Description:
Calcium measurement is critical for numerous biological investigations.
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Catalog Number:
(77977-148)
Supplier:
LGC STANDARDS
Description:
2-[[(3aR,4S,6R,6aS)-6-[[5-Amino-6-chloro-2-(propylthio)-4-pyrimidinyl]amino]tetrahydro-2,2-dimethyl-4H-cyclopenta-1,3-dioxol-4-yl]oxy]ethanol, TRC, LGC Standards
Supplier:
TCI America
Description:
CAS Number: 23628-31-1
MDL Number: MFCD00233711 Molecular Formula: C6H6N2O2 Molecular Weight: 138.13 Purity/Analysis Method: >98.0% (HPLC,T) Form: Crystal Melting point (°C): 315
Supplier:
Spectrum Chemicals
Description:
(Ethylenedinitrilo)tetraacetic Acid, Powder is generally abbreviated as EDTA, a colorless, water soluble, aminopolycarboxylic acid and solid. It's used for its chelating properties and as a ligand. It is used by many industries for application ranging from sequestering agent to chelation therapy. Ungraded products supplied by Spectrum are indicative of a grade suitable for general industrial use or research purposes and typically are not suitable for consumption.
Supplier:
BeanTown Chemical
Description:
CAS: 203866-15-3; MDL No: MFCD03094917
Solid; Molecular Formula: C10H15F2NO4; MW: 251.24
Melting Point: 120-124°
Optical Rotation: [α]22/D -69.0° in chloroform
Supplier:
Bachem Americas
Description:
Sequence: Boc-Arg(Pbf)-OH
Catalog Number:
(EM8.20054.0250)
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
EDTA tetrasodium salt hydrate 98%, pure
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 008762-5G , MDL Number: MFCD01569395
Catalog Number:
(RL200-603-143S)
Supplier:
Rockland Immunochemical
Description:
Anti-D-Amino Acid Oxidase has been assayed against 1.0 µg of D-Amino Acid Oxidase (Pig Kidney) in a standard capture ELISA using ABTS (2,2’-azino-bis-[3-ethylbenthiazoline-6-sulfonic acid])
Supplier:
AMBEED, INC
Description:
PIPES sesquisodium salt 98%
Catalog Number:
(10750-892)
Supplier:
Prosci
Description:
TMEM184B Antibody: TMEM184B, also known as C22orf5, is a 407 amino acid multi-pass membrane protein and represents a novel gene in the activation of the MAPK signaling pathway. The gene encoding TMEM184B maps to human chromosome 22; mutations in several of the genes in chromosome 22 are involved in the development of autism, schizophrenia, Phelan-McDermid syndrome and Neurofibromatosis type 2, suggesting that TMEM184B may play a role in these syndromes.
Catalog Number:
(10311-192)
Supplier:
Bioss
Description:
C22orf43 (chromosome 22 open reading frame 43), also known as MGC33025 or MGC75009, is a 229 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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