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Ace+Method+Development+Kits
Numéro de catalogue:
(PRSI28-107)
Fournisseur:
ProSci Inc.
Description:
VAX1 is a homeo-domain containing protein from a class of homeobox transcription factors which are conserved in vertebrates. It may play an important role in the development of anterior ventral forebrain and visual system.This gene encodes a homeo-domain containing protein from a class of homeobox transcription factors which are conserved in vertebrates. Genes of this family are involved in the regulation of body development and morphogenesis. The most conserved genes, called HOX genes are found in special gene clusters. This gene belongs to the VAX subfamily and lies in the vicinity of the EMX homeobox gene family. Another member of VAX family is located on chromosome 2. The encoded protein may play an important role in the development of anterior ventral forebrain and visual system. Multiple transcript variants encoding different isoforms have been found for this gene.
UOM:
1 * 50 µG
Numéro de catalogue:
(PRSI55-829)
Fournisseur:
ProSci Inc.
Description:
May play a role in sperm development or sperm function.
UOM:
1 * 400 µl
New Product
Numéro de catalogue:
(PRSI92-509)
Fournisseur:
ProSci Inc.
Description:
Fibroblast growth factor 8 (FGF8) is a member of the fibroblast growth factor family. It is discovered as a growth factor essential for the androgen-dependent growth of mouse mammary carcinoma cells. Mouse FGF8b shares 100% aa identity with human FGF8b. FGF8 is widely expressed during embryogenesis, and mediates epithelial-mesenchymal transitions. It plays an important role in the regulation of embryonic development, cell proliferation, cell differentiation and cell migration. It is required for normal brain, eye, ear, limb development during embryogenesis and normal development of the gonadotropin-releasing hormone (GnRH) neuronal system.
UOM:
1 * 50 µG
Numéro de catalogue:
(AATB208)
Fournisseur:
AAT BIOQUEST INC
Description:
6-Carboxy-4'-aminomethylfluorescein is a key building block for developing Big Dye DNA sequencing terminators.
UOM:
1 * 10 mg
New Product
Numéro de catalogue:
(BOSSBS-0052R-A488)
Fournisseur:
Bioss
Description:
Most upstream protease of the activation cascade of caspases responsible for the TNFRSF6/FAS mediated and TNFRSF1A induced cell death. Binding to the adapter molecule FADD recruits it to either receptor. The resulting aggregate called death-inducing signaling complex (DISC) performs CASP8 proteolytic activation. The active dimeric enzyme is then liberated from the DISC and free to activate downstream apoptotic proteases. Proteolytic fragments of the N-terminal propeptide (termed CAP3, CAP5 and CAP6) are likely retained in the DISC. Cleaves and activates CASP3, CASP4, CASP6, CASP7, CASP9 and CASP1. May participate in the GZMB apoptotic pathways. Cleaves ADPRT. Hydrolyzes the small-molecule substrate, Ac-Asp-Glu-Val-Asp-|-AMC. Likely target for the cowpox virus CRMA death inhibitory protein.
UOM:
1 * 100 µl
Numéro de catalogue:
(PRSI91-922)
Fournisseur:
ProSci Inc.
Description:
Phosphoinositide-3-kinase-interacting protein 1(PIK3IP1) is an enzyme that in humans is encoded by the PIK3IP1 gene.It is a negative regulator of phosphatidylinositol-3-kinase (PI3K), suppresses the development of hepatocellular carcinoma. The gene encoding PIK3IP1 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.
UOM:
1 * 50 µG
Numéro de catalogue:
(PRSI27-240)
Fournisseur:
ProSci Inc.
Description:
SOX8 is a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. It may act as a transcriptional activator after forming a protein complex with other proteins. This protein may be involved in brain development and function. Haploinsufficiency for this protein may contribute to the mental retardation found in haemoglobin H-related mental retardation (ART-16 syndrome).This gene encodes a member of the SOX (SRY-related HMG-box) family of transcription factors involved in the regulation of embryonic development and in the determination of the cell fate. The encoded protein may act as a transcriptional activator after forming a protein complex with other proteins. This protein may be involved in brain development and function. Haploinsufficiency for this protein may contribute to the mental retardation found in haemoglobin H-related mental retardation (ART-16 syndrome).
UOM:
1 * 50 µG
Numéro de catalogue:
(PRSI28-760)
Fournisseur:
ProSci Inc.
Description:
Lmx1a acts as a transcriptional activator by binding to an A/T-rich sequence, the FLAT element, in the insulin gene promoter. It is required for development of the roof plate and, in turn, for specification of dorsal cell fates in the CNS and developing vertebrae.
UOM:
1 * 1 EA
Numéro de catalogue:
(PRSI28-982)
Fournisseur:
ProSci Inc.
Description:
FOXB1 is a winged helix/forkhead transcription factor. FOXB1 is specifically expressed in the developing central nervous system (CNS). Early embryonic FOXB1 expression is restricted to the mammiliary body region of the caudal hypothalamus, midbrain, hindbrain and spinal cord. FOXB1 may play a role in postnatal growth, lactation and CNS development.
UOM:
1 * 1 EA
Numéro de catalogue:
(AATB17672)
Fournisseur:
AAT BIOQUEST INC
Description:
Hoechst 33342 maleimide is an excellent building block for developing site-specific nucleic acid probes.
UOM:
1 * 1 mg
New Product
Numéro de catalogue:
(AATB17671)
Fournisseur:
AAT BIOQUEST INC
Description:
Hoechst 33342 amine is an excellent building block for developing site-specific nucleic acid probes.
UOM:
1 * 1 mg
New Product
Numéro de catalogue:
(PRSI29-450)
Fournisseur:
ProSci Inc.
Description:
In mammals, the Y chromosome directs the development of the testes and plays an important role in spermatogenesis. A high percentage of infertile men have deletions that map to regions of the Y chromosome. The DAZ (deleted in azoospermia) gene cluster maps to the AZFc region of the Y chromosome and is deleted in many azoospermic and severely oligospermic men. It is thought that the DAZ gene cluster arose from the transposition, amplification, and pruning of the ancestral autosomal gene DAZL also involved in germ cell development and gametogenesis. DAZAP1 is a RNA-binding protein with two RNP motifs that was originally identified by its interaction with the infertility factors DAZ and DAZL.In mammals, the Y chromosome directs the development of the testes and plays an important role in spermatogenesis. A high percentage of infertile men have deletions that map to regions of the Y chromosome. The DAZ (deleted in azoospermia) gene cluster maps to the AZFc region of the Y chromosome and is deleted in many azoospermic and severely oligospermic men. It is thought that the DAZ gene cluster arose from the transposition, amplification, and pruning of the ancestral autosomal gene DAZL also involved in germ cell development and gametogenesis. This gene encodes a RNA-binding protein with two RNP motifs that was originally identified by its interaction with the infertility factors DAZ and DAZL. Two isoforms are encoded by transcript variants of this gene.In mammals, the Y chromosome directs the development of the testes and plays an important role in spermatogenesis. A high percentage of infertile men have deletions that map to regions of the Y chromosome. The DAZ (deleted in azoospermia) gene cluster maps to the AZFc region of the Y chromosome and is deleted in many azoospermic and severely oligospermic men. It is thought that the DAZ gene cluster arose from the transposition, amplification, and pruning of the ancestral autosomal gene DAZL also involved in germ cell development and gametogenesis. This gene encodes a RNA-binding protein with two RNP motifs that was originally identified by its interaction with the infertility factors DAZ and DAZL. Two isoforms are encoded by transcript variants of this gene.
UOM:
1 * 1 EA
Numéro de catalogue:
(PRSI27-748)
Fournisseur:
ProSci Inc.
Description:
BARX1 belongs to the Bar subclass of the homeobox gene family. The function of this gene has not yet been determined; however, studies in the mouse and chick homolog suggest a role in developing teeth and craniofacial mesenchyme of neural crest origin. The role of these homologs implicates the human gene as a candidate for unmapped disorders involving tooth and jaw development.
UOM:
1 * 50 µG
Numéro de catalogue:
(AATB1154)
Fournisseur:
AAT BIOQUEST INC
Description:
mFluor™ dyes are developed for multicolor flow cytometry-focused applications.
UOM:
1 * 1 mg
New Product
Numéro de catalogue:
(LIEDPR335D)
Fournisseur:
LIEDER JOHANNES
Description:
These preparations are designed for educational purposes.
UOM:
1 * 1 ST
Numéro de catalogue:
(AATB702)
Fournisseur:
AAT BIOQUEST INC
Description:
Bodi Fluor 488 amine is an excellent building block for developing fluorescent probes.
UOM:
1 * 5 mg
New Product
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