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Yttrium(III)+fluoride
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Yttrium(III)+fluoride
Catalog Number:
(103309-830)
Supplier:
Novus Biologicals
Description:
The SCN3A Antibody (3F3) from Novus Biologicals is a mouse monoclonal antibody to SCN3A. This antibody reacts with human. The SCN3A Antibody (3F3) has been validated for the following applications: Western Blot, ELISA.
Catalog Number:
(89357-970)
Supplier:
Genetex
Description:
This gene encodes a member of the annexin family. Members of this calcium-dependent phospholipid-binding protein family play a role in the regulation of cellular growth and in signal transduction pathways. This protein functions in the inhibition of phopholipase A2 and cleavage of inositol 1,2-cyclic phosphate to form inositol 1-phosphate. This protein may also play a role in anti-coagulation. [provided by RefSeq]
Catalog Number:
(103271-652)
Supplier:
Novus Biologicals
Description:
The ACY3 Antibody from Novus Biologicals is a rabbit polyclonal antibody to ACY3. This antibody reacts with human. The ACY3 Antibody has been validated for the following applications: Western Blot, Immunohistochemistry, Immunocytochemistry / Immunofluorescence, Immunohistochemistry-Paraffin.
Catalog Number:
(10449-444)
Supplier:
Bioss
Description:
The protein encoded by this gene belongs to the leucine-rich repeat superfamily. This gene was found to be amplified and overexpressed in malignant gliomas. The encoded protein has homology with other proteins that function as cell-adhesion molecules or as signal transduction receptors and is a candidate for the target gene in the 1q32.1 amplicon in malignant gliomas. Two alternatively spliced transcript variants encoding the same protein have been described for this gene.
Catalog Number:
(103633-514)
Supplier:
Sino Biological
Description:
A DNA sequence encoding the envelope protein of West Nile Virus (WNV) (lineage 2, strain Nea Santa-Greece-2010) (AED99787.1 ) (Gln586-Ala705) was expressed with a polyhistidine tag at the C-terminus.
Catalog Number:
(10349-932)
Supplier:
Bioss
Description:
The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII often referred to as the `pure' cerebellar syndrome (SCA5), are most likely homogeneous disorders. Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions. ADCA is caused by the expansion of the CAG repeats, producing an elongated polyglutamine tract in the corresponding protein. The expanded repeats are variable in size and unstable, usually increasing in size when transmitted to successive generations. The function of the ataxins is not known. This locus has been mapped to chromosome 6, and it has been determined that the diseased allele contains41-81 CAG repeats, compared to 6-39 in the normal allele, and is associated with spinocerebellar ataxia type 1 (SCA1). At least two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq].
Catalog Number:
(10349-942)
Supplier:
Bioss
Description:
The autosomal dominant cerebellar ataxias (ADCA) are a heterogeneous group of neurodegenerative disorders characterized by progressive degeneration of the cerebellum, brain stem and spinal cord. Clinically, ADCA has been divided into three groups: ADCA types I-III. ADCAI is genetically heterogeneous, with five genetic loci, designated spinocerebellar ataxia (SCA) 1, 2, 3, 4 and 6, being assigned to five different chromosomes. ADCAII, which always presents with retinal degeneration (SCA7), and ADCAIII often referred to as the `pure' cerebellar syndrome (SCA5), are most likely homogeneous disorders. Several SCA genes have been cloned and shown to contain CAG repeats in their coding regions. ADCA is caused by the expansion of the CAG repeats, producing an elongated polyglutamine tract in the corresponding protein. The expanded repeats are variable in size and unstable, usually increasing in size when transmitted to successive generations. The function of the ataxins is not known. This locus has been mapped to chromosome 6, and it has been determined that the diseased allele contains41-81 CAG repeats, compared to 6-39 in the normal allele, and is associated with spinocerebellar ataxia type 1 (SCA1). At least two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq].
Catalog Number:
(103634-754)
Supplier:
Sino Biological
Description:
Produced in rabbits immunized with purified, recombinant Human REG3G (rh REG3G; Catalog#11641-H08H; NP_001008388.1; Met 1-Asp 175). Total IgG was purified by Protein A affinity chromatography
.
Catalog Number:
(103309-832)
Supplier:
Novus Biologicals
Description:
The SCN3A Antibody (2F8) from Novus Biologicals is a mouse monoclonal antibody to SCN3A. This antibody reacts with human. The SCN3A Antibody (2F8) has been validated for the following applications: Western Blot, ELISA.
Catalog Number:
(EM1.01047.1000)
Supplier:
IBI Scientific
Description:
EDTA is commonly used in biological and electrophoresis buffer systems.
Catalog Number:
(10300-516)
Supplier:
Bioss
Description:
The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter’s syndrome which is characterized by renal salt-wasting and low blood pressure.
Catalog Number:
(10303-570)
Supplier:
Bioss
Description:
The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter’s syndrome which is characterized by renal salt-wasting and low blood pressure.
Catalog Number:
(76304-288)
Supplier:
PeproTech, Inc.
Description:
NAP-2 is a CXC chemokine that can signal through the CXCR1 and CXCR2 receptors. It is produced in leukocytes by enzymatic processing of a precursor called platelet basic protein (PBP). NAP-2 chemoattracts and activates neutrophils. Recombinant Human NAP-2 protein is a 7.6 kDa protein containing 70 amino acid residues, including the four highly conserved cysteine residues present in CXC chemokines, and also the "ELR" motif, common to CXC chemokines that bind to CXCR1 and CXCR2.
Catalog Number:
(103633-390)
Supplier:
Sino Biological
Description:
A DNA sequence encoding the envelope protein of Dengue virus (DENV)(type 2, strain New Guinea C/PUO-218 hybrid)(AAC59274.1) (Met578-Gln680) was expressed with a polyhistidine tag at the C-terminus.
Supplier:
Thermo Scientific Chemicals
Description:
In printing, fabrics, dyeing, manufacturing of paper, vegetable glue, baking powder, purifying water, clarifying sugar, as catalyst in ammonia synthesis, hardening agent in microscopy
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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.
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