Anticorps
Numéro de catalogue:
(USBI036309-FITC)
Fournisseur:
US Biological
Description:
Anti-GRIP2 Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))
UOM:
1 * 200 µl
Numéro de catalogue:
(USBI036464-APC)
Fournisseur:
US Biological
Description:
Anti-hCG_2039146 Rabbit Polyclonal Antibody (APC (Allophycocyanin))
UOM:
1 * 200 µl
Numéro de catalogue:
(USBI150251)
Fournisseur:
US Biological
Description:
Anti-CHRNB3 Goat Polyclonal Antibody
UOM:
1 * 1 EA
Numéro de catalogue:
(USBIC2262-35T)
Fournisseur:
US Biological
Description:
Anti-ITGAM Mouse Monoclonal Antibody (Biotin) [clone: 7H195]
UOM:
1 * 1 EA
Numéro de catalogue:
(USBIC2100-10)
Fournisseur:
US Biological
Description:
Anti-CCR9 Goat Polyclonal Antibody
UOM:
1 * 1 EA
Numéro de catalogue:
(USBIC2262-36E)
Fournisseur:
US Biological
Description:
Anti-ITGAM Mouse Monoclonal Antibody [clone: 8J256]
UOM:
1 * 500 µG
Numéro de catalogue:
(USBIB2553-33A-APC)
Fournisseur:
US Biological
Description:
Anti-BMP7 Rabbit Polyclonal Antibody (APC (Allophycocyanin))
UOM:
1 * 200 µl
Numéro de catalogue:
(USBIC2100-02F)
Fournisseur:
US Biological
Description:
Anti-CCR8 Rabbit Polyclonal Antibody
UOM:
1 * 50 µG
Numéro de catalogue:
(USBIB2553-20H-HRP)
Fournisseur:
US Biological
Description:
Anti-BMP4 Rabbit Polyclonal Antibody (HRP (Horseradish Peroxidase))
UOM:
1 * 200 µl
Numéro de catalogue:
(USBIC2262-35K)
Fournisseur:
US Biological
Description:
Anti-ITGAM Rat Monoclonal Antibody (PE (Phycoerythrin)) [clone: 5K8]
UOM:
1 * 1 EA
Numéro de catalogue:
(BOSSBS-8216R)
Fournisseur:
Bioss
Description:
Isoform 1 and isoform 3 are widely expressed with highest levels in retina and testis, with isoform 1 being the mot abundant in all tissues tested.Involvement in disease:Defects in FAM161A are the cause of retinitis pigmentosa type 28 (RP28) . A retinal dystrophy belonging to the group of pigmentary retinopathies. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-8196R)
Fournisseur:
Bioss
Description:
Anti-NXPE4 Rabbit Polyclonal Antibody
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-8215R)
Fournisseur:
Bioss
Description:
FAM13C1, also known as FAM13C, is a 585 amino acid protein that belongs to the FAM13 family. Existing as three alternatively spliced isoforms, the gene encoding FAM13C1 maps to human chromosome 10, which contains over 800 genes, 135 million nucleotides and makes up nearly 4.5% of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-8200R)
Fournisseur:
Bioss
Description:
Differentiation of myogenic cells is regulated by multiple positively and negatively acting factors. One well characterized family of helix-loop-helix (HLH) proteins known to play an important role in the regulation of muscle cell development include Myo D, myogenin, Myf-5 and Myf-6 (also designated MRF-4 or herculin). Of interest, most muscle cells express either Myo D or Myf-5 in the committed state, but when induced to differentiate, all turn on expression of myogenin. Myo D transcription factors form heterodimers with products of a more widely expressed family of bHLH genes, the E family, which consists of at least three distinct genes: E2A, IF2 and HEB. Myo D-E heterodimers bind avidly to consensus (CANNTG) E box target sites that are functionally important elements in the upstream regulatory sequences of many muscle-specific terminal differentiation genes.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9319R)
Fournisseur:
Bioss
Description:
NNF1R, also called PMF1, is part of the MIS12 complex, which may be fundamental for kinetochore formation and proper chromosome segregation during mitosis. It is required for chromosome congression and for correct operation of the spindle checkpoint. May act as a cotranscription partner of NFE2L2 involved in regulation of polyamine-induced transcription of SSAT.
UOM:
1 * 100 µl
Numéro de catalogue:
(BOSSBS-9348R)
Fournisseur:
Bioss
Description:
ACLP2 (acid phosphatase-like 2), also known as UNQ370 or PRO706, is a 480 amino acid secreted protein that functions to catalyze the H2O-dependent conversion of a phosphate monoester to an alcohol and a phosphate. Expressed as two alternatively spliced isoforms, ACPL2 is encoded by a gene that maps to chromosome 3, which houses over 1,100 genes, including a chemokine receptor (CKR) gene cluster and a variety of human cancer-related gene loci. Key tumor suppressing genes on chromosome 3 include those that encode the apoptosis mediator RASSF1, the cell migration regulator HYAL1 and the angiogenesis suppressor SEMA3B. Marfan Syndrome, porphyria, von Hippel-Lindau syndrome, osteogenesis imperfecta and Charcot-Marie-Tooth Disease are a few of the numerous genetic diseases associated with chromosome 3.
UOM:
1 * 100 µl
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