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2,2-Difluoropropionic+acid
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2,2-Difluoropropionic+acid
Supplier:
Justrite
Description:
Justrite's exclusive ChemCor® Lined Acid Safety Cabinets are available in standard 30, 45, and 60 gallon (114, 170 and 227 L) sizes, as well as slimline, compac, countertop, undercounter and piggyback styles.
Supplier:
MP Biomedicals
Description:
Essential vitamin that is important for amino acid and energy metabolism, and fatty acid synthesis. It is a prosthetic group in four mammalian carboxylase families and facilitates the binding and transfer of carbon dioxide.
Catalog Number:
(75932-958)
Supplier:
Rockland Immunochemical
Description:
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.
Supplier:
AMBEED, INC
Description:
2,4,6-Triisopropylphenylboronic acid dimethyl ester 95+%
Catalog Number:
(89515-542)
Supplier:
Abgent
Description:
polyclonal antibody Isotype: Rabbit Ig, Species Reactivity: human, Gene ID: 5675, Target/specificity: This PSG6 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 22-48 amino acids from the N-terminal region of human PSG6.
Catalog Number:
(10310-196)
Supplier:
Bioss
Description:
C22orf37 (chromosome 22 open reading frame 37), also known as FLJ40542, is a 170 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:
Matrix Scientific Part Number: 043268-5G , MDL Number: MFCD06659535
Catalog Number:
(10761-720)
Supplier:
Biolegend
Description:
Purified anti-mouse IL-22 [Poly5164]; Isotype: Goat Polyclonal IgG; Reactivity: Mouse; Apps: ELISA Capture; Size: 100 μg
Catalog Number:
(101924-878)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 062957-500MG , MDL Number: MFCD06624152
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
4-Hydroxy-3-methoxyphenylboronic acid pinacol ester 97%
Catalog Number:
(10761-714)
Supplier:
Biolegend
Description:
Biotin anti-human IL-22 [Poly5161]; Isotype: Goat Polyclonal Ig; Reactivity: Human; Apps: ELISA Detection; Size: 50 μg
Supplier:
BeanTown Chemical
Description:
CAS: 1120-71-4; EC No: 214-317-9; MDL No: MFCD00005355; RTECS: RP5425000
UN No: UN2811; Haz Class: 6.1; Packing Group: III
Solid; Molecular Formula: C3H6O3S; MW: 122.14
Melting Point: 30-33°; Boiling Point: 180°/30 mmHg; Flash point: 110°C (230°F)
Density (g/mL): 1.392
Moisture Sensitive
Catalog Number:
(101850-032)
Supplier:
Matrix Scientific
Description:
Matrix Scientific Part Number: 040715-500MG , MDL Number: MFCD06010034
Catalog Number:
(PI25003)
Supplier:
Invitrogen
Description:
Thermo Scientific Pierce Heptafluorobutyric Acid (HFBA) is manufactured and tested to meet strict specifications that ensure superior performance for use as an ion-pairing agent.
Catalog Number:
(10311-194)
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.
Catalog Number:
(89519-140)
Supplier:
Abgent
Description:
Polyclonal Antibody, Isotype: Rabbit Ig, Species Reactivity: Human, Gene ID: 1146, Target/Specificity: generated from rabbits immunized with a KLH conjugated synthetic peptide between 22-50 amino acids from the N-terminal region of human CHRNG
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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.
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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