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2,2\\\\\\\'-[ethylenebis(oxy)]bisacetic+acid
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2,2\\\\\\\'-[ethylenebis(oxy)]bisacetic+acid
Supplier:
AOB CHEM USA
Description:
1-Bromo-4-((4-methoxybenzyl)oxy)benzene ≥97%
Supplier:
AOB CHEM USA
Description:
3-Chloro-4-((4-fluorobenzyl)oxy)phenol ≥97%
Catalog Number:
(76120-458)
Supplier:
Bioss
Description:
Ankyrins are membrane adaptor molecules that play important roles in coupling integral membrane proteins to the spectrin-based cytoskeleton network. Mutations of ankyrin genes lead to severe genetic diseases such as fatal cardiac arrhythmias and hereditary spherocytosis. ANKRD20A (ankyrin repeat domain-containing protein 20A) is an 823 amino acid protein that contains five ANK repeats. The gene encoding ANKRD20A maps to chromosome 9, which consists of about 145 million bases and encodes nearly 900 genes. Considered to play a role in gender determination, deletion of the distal portion of 9p can lead to development of male to female sex reversal, the phenotype of a female with a male X,Y genotype. Hereditary hemorrhagic telangiectasia, which is characterized by harmful vascular defects, and familial dysautonomia are associated with chromosome 9. Also, chromosome 9 is partnered with chromosome 22 in the translocation leading to the aberrant production of BCR-ABL fusion protein often found in leukemias.
Catalog Number:
(RL100-1137)
Supplier:
Rockland Immunochemical
Description:
Anti-glucose oxidase antibody has been assayed against 1.0 µg of Glucose Oxidase (Aspergillus niger) in a standard ELISA using Peroxidase conjugated Affinity Purified anti-Goat IgG and ABTS (2,2’-azino-bis-[3-ethylbenthiazoline-6-sulfonic acid])
Supplier:
THERMO FISHER SCIENTIFIC CHEMICALS
Description:
EDTA dipotassium salt dihydrate 99%, Extra Pure
Supplier:
TCI America
Description:
CAS Number: 5006-62-2
MDL Number: MFCD00005991 Molecular Formula: C8H15NO2 Molecular Weight: 157.21 Purity/Analysis Method: >98.0% (GC,T) Form: Clear Liquid Boiling point (°C): 104 Flash Point (°C): 90 Specific Gravity (20/20): 1.02
Supplier:
AMBEED, INC
Description:
3-((2-Isopropyl-5-methylcyclohexyl)oxy)propane-1,2-diol 97%
Catalog Number:
(101929-458)
Supplier:
Matrix Scientific
Description:
MF=C14H24O2 MW=224.35 MDL=MFCD19103272 500Mg
Supplier:
AMBEED, INC
Description:
2-(4-((2,5-Difluorobenzyl)oxy)phenoxy)-5-ethoxyaniline 98%
Catalog Number:
(103666-898)
Supplier:
Sino Biological
Description:
A DNA sequence encoding the mature form of mouse CXCL9 (P18340) (Thr 22-Thr 126) was expressed, with an initial Met at the C-terminus.
Supplier:
AOB CHEM USA
Description:
Methyl 2-[(6-bromo-2-pyridinyl)oxy]-2-methylpropanoate ≥97%
Catalog Number:
(89415-496)
Supplier:
Prosci
Description:
IL-22 Receptor Antibody: A novel cytokine, designated IL-TIF for IL-10 related T cell-derived inducible factor and IL-22, was recently identified. The receptor for IL-22 (IL-22R, also termed CRF2-9 and IL-TIF-R1 chain) is a new member of the class II cytokine receptor family. IL-22R forms a complex with IL-10 receptor beta chain and mediates IL-22 signaling. IL-22 and its receptor activate JAK-STAT signaling pathway. IL22R is expressed in normal liver and kidney and their cell lines HepG2 and TK-10. A soluble form of IL-22 receptor, also termed IL-22 binding protein (IL-22BP) and IL-22 receptor-alpha 2 (IL-22RA2), was identified very recently. IL-22BP prevents binding of IL-22 to the functional cell surface IL-22R complex and neutralizes IL-22 activity. LPS induces IL-22 expression, which indicates the role of IL-22 in inflammatory response.
Catalog Number:
(10254-274)
Supplier:
Bioss
Description:
SNAP 29 is a 258 amino acid protein that localizes to the membrane and the cytoplasm, as well as to the cell junction, and contains one t-SNARE coiled-coil homology domain. Expressed in liver, heart, brain, kidney, placenta, lung, spleen, pancreas and skeletal muscle, SNAP 29 binds tightly to Syntaxins and, via this binding, is involved in membrane trafficking events. Defects in the gene encoding SNAP 29 are the cause of CEDNIK syndrome, a neurocutaneous syndrome that is associated with cerebral dysgenesis, neuropathy, ichthyosis and palmoplantar keratoderma. The gene encoding SNAP 29 maps to human 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.
Catalog Number:
(10254-262)
Supplier:
Bioss
Description:
SNAP 29 is a 258 amino acid protein that localizes to the membrane and the cytoplasm, as well as to the cell junction, and contains one t-SNARE coiled-coil homology domain. Expressed in liver, heart, brain, kidney, placenta, lung, spleen, pancreas and skeletal muscle, SNAP 29 binds tightly to Syntaxins and, via this binding, is involved in membrane trafficking events. Defects in the gene encoding SNAP 29 are the cause of CEDNIK syndrome, a neurocutaneous syndrome that is associated with cerebral dysgenesis, neuropathy, ichthyosis and palmoplantar keratoderma. The gene encoding SNAP 29 maps to human 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.
Catalog Number:
(10254-282)
Supplier:
Bioss
Description:
SNAP 29 is a 258 amino acid protein that localizes to the membrane and the cytoplasm, as well as to the cell junction, and contains one t-SNARE coiled-coil homology domain. Expressed in liver, heart, brain, kidney, placenta, lung, spleen, pancreas and skeletal muscle, SNAP 29 binds tightly to Syntaxins and, via this binding, is involved in membrane trafficking events. Defects in the gene encoding SNAP 29 are the cause of CEDNIK syndrome, a neurocutaneous syndrome that is associated with cerebral dysgenesis, neuropathy, ichthyosis and palmoplantar keratoderma. The gene encoding SNAP 29 maps to human 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.
Catalog Number:
(103665-030)
Supplier:
Sino Biological
Description:
A DNA sequence encoding the mouse EGFL7 isoform 1 (Q9QXT5-1) (Glu 22-Leu 275) was fused with a polyhistidine tag at the N-terminus.
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 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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