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Ace+Method+Development+Kits
Numéro de catalogue:
(PRSI40-605)
Fournisseur:
ProSci Inc.
Description:
Keratinocyte Growth Factor (KGF/FGF-7) is one of 23 known members of the FGF family. Proteins of this family play a central role during prenatal development and postnatal growth and regeneration of variety of tissues, by promoting cellular proliferation and differentiation. KGF/FG-7 is a mitogen factor specific for epithelial cells and keratinocytes and signals through FGFR 2b. KGF/FGF-7 plays a role in kidney and lung development, angiogenesis, and wound healing. Recombinant human KGF/FGF-7 is an 18.9 kDa protein consisting of 163 amino acid residues.
UOM:
1 * 1 EA
Numéro de catalogue:
(AATB50015)
Fournisseur:
AAT BIOQUEST INC
Description:
3-Amino-5-morpholinomethyl-2-oxazolidinone (AMOZ)-HRP conjugate is used for developing an ELISA assay for quantifying 3-Amino-5-morpholinomethyl-2-oxazolidinone (AMOZ).
UOM:
1 * 1 mg
New Product
Numéro de catalogue:
(PRSI25-038)
Fournisseur:
ProSci Inc.
Description:
MNX1 contains 1 homeobox DNA-binding domain. MNX1 is a putative transcription factor involved in pancreas development and function. Defects in MNX1 are a cause of Currarino syndrome.
UOM:
1 * 50 µG
Numéro de catalogue:
(PRSI91-949)
Fournisseur:
ProSci Inc.
Description:
It is a single-pass type I membrane protein and contains 4 TNFR-Cys repeats. The protein is a member of the tumor necrosis factor (TNF) family of receptors. It is expressed on the surface of most cell types, including cells of epithelial and myeloid lineages, but not on T and B lymphocytes. The protein is the receptor for the heterotrimeric lymphotoxin containing LTA and LTB, and for TNFS14/LIGHT. It promotes apoptosis via TRAF3 and TRAF5 and may play a role in the development of lymphoid organs. The encoded protein and its ligand play a role in the development and organization of lymphoid tissue and transformed cells. Activation of the encoded protein can trigger apoptosis. Not only does the TNFRSF3 help trigger apoptosis, it can lead to the release of the cytokine interleukin 8. Overexpression of TNFRSF3 in Human Cells cells increases IL-8 promoter activity and leads to IL-8 release. TNFRSF3 is also essential for development and organization of the secondary lymphoid organs and chemokine release.
UOM:
1 * 50 µG
Numéro de catalogue:
(PRSI55-640)
Fournisseur:
ProSci Inc.
Description:
This gene encodes a member of the homeodomain-containing superfamily of transcription factors. The protein binds to DNA as either a homodimer, or a heterodimer with the related protein hepatocyte nuclear factor 1-alpha. The gene has been shown to function in nephron development, and regulates development of the embryonic pancreas. Mutations in this gene result in renal cysts and diabetes syndrome and noninsulin-dependent diabetes mellitus, and expression of this gene is altered in some types of cancer. Multiple transcript variants encoding different isoforms have been found for this gene.
UOM:
1 * 400 µl
New Product
Numéro de catalogue:
(PRSI27-572)
Fournisseur:
ProSci Inc.
Description:
SIX6 is a member of SIX family. It is the homologue of the chick Six6 (Optx2) gene. SIX6 is closely related to SIX3 and is expressed in the developing and adult human retina.
UOM:
1 * 50 µG
Numéro de catalogue:
(PRSI29-803)
Fournisseur:
ProSci Inc.
Description:
IRX3 is a member of the Iroquois homeobox gene family that encodes a protein known for its essential role in spinal cord development.
UOM:
1 * 50 µG
Numéro de catalogue:
(PRSI56-058)
Fournisseur:
ProSci Inc.
Description:
Probable E3 ubiquitin-protein ligase which plays an important role in blastocyst development (By similarity).
UOM:
1 * 400 µl
New Product
Numéro de catalogue:
(PRSI26-329)
Fournisseur:
ProSci Inc.
Description:
CpG methylation is an epigenetic modification that is important for embryonic development, imprinting, and X-chromosome inactivation. Studies in mice have demonstrated that DNA methylation is required for mammalian development. TRDMT1 is a protein with similarity to DNA methyltransferases, but this protein does not display methyltransferase activity. The protein strongly binds DNA, suggesting that it may mark specific sequences in the genome.CpG methylation is an epigenetic modification that is important for embryonic development, imprinting, and X-chromosome inactivation. Studies in mice have demonstrated that DNA methylation is required for mammalian development. This gene encodes a protein with similarity to DNA methyltransferases, but this protein does not display methyltransferase activity. The protein strongly binds DNA, suggesting that it may mark specific sequences in the genome. Alternative splicing results in multiple transcript variants encoding different isoforms.
UOM:
1 * 50 µG
Numéro de catalogue:
(PRSI27-818)
Fournisseur:
ProSci Inc.
Description:
ZNF212 belongs to the C2H2-type zinc finger gene family. The zinc finger proteins are involved in gene regulation and development, and are quite conserved throughout evolution.
UOM:
1 * 50 µG
Numéro de catalogue:
(PRSI31-317)
Fournisseur:
ProSci Inc.
Description:
LRRTM1 may play a role during the development of specific forebrain structures by influencing neuronal differentiation and connectivity, with a possible role in intracellular trafficking within axons.
UOM:
1 * 50 µG
Numéro de catalogue:
(PRSI25-577)
Fournisseur:
ProSci Inc.
Description:
BCL6B acts as a sequence-specific transcriptional repressor in association with BCL6. BCL6B may function in a narrow stage or be related to some events in the early B-cell development.
UOM:
1 * 50 µG
Numéro de catalogue:
(PRSI27-307)
Fournisseur:
ProSci Inc.
Description:
PDPK1 phosphorylates and activates not only PKB/AKT, but also PKA, PKC-zeta, RPS6KA1 and RPS6KB1. It may play a general role in signaling processes and in development.
UOM:
1 * 50 µG
Numéro de catalogue:
(PRSI27-861)
Fournisseur:
ProSci Inc.
Description:
The NR2E1 gene is a member of the steroid nuclear receptor superfamily and is predominately expressed in the brain. The contributions of this gene to human B-cell leukemia and to brain development are unknown at present.
UOM:
1 * 50 µG
Numéro de catalogue:
(PRSI25-067)
Fournisseur:
ProSci Inc.
Description:
EYA1 is a member of the eyes absent (EYA) family of proteins. EYA1 may play a role in the developing kidney, branchial arches, eye, and ear. Mutations of this gene have been associated with branchiootorenal dysplasia syndrome, branchiootic syndrome, and sporadic cases of congenital cataracts and ocular anterior segment anomalies. A similar protein in mice can act as a transcriptional activator.This gene encodes a member of the eyes absent (EYA) family of proteins. The encoded protein may play a role in the developing kidney, branchial arches, eye, and ear. Mutations of this gene have been associated with branchiootorenal dysplasia syndrome, branchiootic syndrome, and sporadic cases of congenital cataracts and ocular anterior segment anomalies. A similar protein in mice can act as a transcriptional activator. Four transcript variants encoding three distinct isoforms have been identified for this gene.
UOM:
1 * 50 µG
Numéro de catalogue:
(PRSI30-149)
Fournisseur:
ProSci Inc.
Description:
The catalytic conversion of UTP to CTP is accomplished by the enzyme cytidine-5-prime-triphosphate synthetase. The enzyme is important in the biosynthesis of phospholipids and nucleic acids, and plays a key role in cell growth, development, and tumorigenesis.The catalytic conversion of UTP to CTP is accomplished by the enzyme cytidine-5-prime-triphosphate synthetase. The enzyme is important in the biosynthesis of phospholipids and nucleic acids, and plays a key role in cell growth, development, and tumorigenesis. The region to which the CTPS gene has been mapped is the location of breakpoints involved in several tumor types.
UOM:
1 * 1 EA
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