Benefits of using C-Chips
• Disposable
• Coverslips not required
• Washing and reuse time eradicated
• Publicity to infectious samples and contamination decreased
• Repeatability and reliability assured
• Sturdy and strong – quartz grade optical plastic used
• Two exams per slide
Features
• Blood cell counting
• Cell focus measurement
• Cell viability check out
• Micro organism and fungal spore counting IVF, IUI
• Sperm counting
Fashions
• Neubauer Improved (100 µm depth) – DHC-N01
• Fuchs Rosenthal (200 µm depth) – DHC-F01
• Burker (100 µm depth) – DHC-B01
• Burker Turk (100 µm depth) – DHC-B02
• Malassez (200 µm depth) – DHC-M01
EVE slides
Slides appropriate with the EVE cell counter

Merchandise
Observe: Product availability is set by the nation – see the product aspect net web page.
Particulars | Cat amount & supplier | Dimension | Worth |
Neubauer Improved C-Chip Disposable Haemocytometer (2 channel) |
DHC-N01
NanoEnTek |
1000 slides | £1265.00view |
Fuchs Rosenthal C-Chip Disposable Haemocytometer (2 channel) |
DHC-F01
NanoEnTek |
1000 slides | £1265.00view |
Burker C-Chip Disposable Haemocytometer (2 channel) |
DHC-B01
NanoEnTek |
1000 slides | £1265.00view |
Burker Turk C-Chip Disposable Haemocytometer (2 channel) |
DHC-B02
NanoEnTek |
1000 slides | £1265.00view |
Malassez C-Chip Disposable Haemocytometer (2 channel) |
DHC-M01
NanoEnTek |
1000 slides | £1265.00view |
Neubauer Improved C-Chip Disposable Haemocytometer (2 channel) |
DHC-N01-50
NanoEnTek |
50 slides | £65.00view |
Fuchs Rosenthal C-Chip Disposable Haemocytometer (2 channel) |
DHC-F01-50
NanoEnTek |
50 slides | £65.00view |
Burker C-Chip Disposable Haemocytometer (2 channel) |
DHC-B01-50
NanoEnTek |
50 slides | £65.00view |
Malassez C-Chip Disposable Haemocytometer (2 channel) |
DHC-M01-50
NanoEnTek |
50 slides | £65.00view |
Choices and benefits
- No should coverslip.
- No need to clear for reuse.
- No additional contact to hazardous provides (e.g. AIDS affected individual blood, urine).
- Appropriate, reliable and repeatable.
- Sensible grid pattern.
- Quartz grade optical plastic.
- Sturdy and strong.
Basic functions:
- Blood analysis.
- Cell custom; cell focus measurement and cell viability counts.
- Microbiology; bacterial and fungal spores.
- IVF, IUI; sperm counts.
ARHGDIA Antibody / RHOGDI Antibody |
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F54788-0.4ML | NSJ Bioreagents | 0.4 ml | EUR 322.15 |
Description: ARHGDIA regulates the GDP/GTP exchange reaction of the Rho proteins by inhibiting the dissociation of GDP from them, and the subsequent binding of GTP to them. |
CLCN5 Antibody / CIC-5 antibody |
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RQ6462 | NSJ Bioreagents | 100ug | EUR 356.15 |
Description: The CLCN5 gene encodes the chloride channel Cl-/H+ exchanger ClC-5. This gene encodes a member of the ClC family of chloride ion channels and ion transporters. The encoded protein is primarily localized to endosomal membranes and may function to facilitate albumin uptake by the renal proximal tubule. Mutations in this gene have been found in Dent disease and renal tubular disorders complicated by nephrolithiasis. Alternatively spliced transcript variants have been found for this gene. |
Anti-Anti-SEPT5 Antibody antibody |
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STJ114819 | St John's Laboratory | 100 µl | EUR 332.4 |
Description: This gene is a member of the septin gene family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is mapped to 22q11, the region frequently deleted in DiGeorge and velocardiofacial syndromes. A translocation involving the MLL gene and this gene has also been reported in patients with acute myeloid leukemia. Alternative splicing results in multiple transcript variants. The presence of a non-consensus polyA signal (AACAAT) in this gene also results in read-through transcription into the downstream neighboring gene (GP1BB; platelet glycoprotein Ib), whereby larger, non-coding transcripts are produced. |
Anti-Anti-SEPT2 Antibody antibody |
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STJ28365 | St John's Laboratory | 100 µl | EUR 332.4 |
Anti-Anti-SEPT7 Antibody antibody |
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STJ28963 | St John's Laboratory | 100 µl | EUR 332.4 |
Description: This gene encodes a protein that is highly similar to the CDC10 protein of Saccharomyces cerevisiae. The protein also shares similarity with Diff 6 of Drosophila and with H5 of mouse. Each of these similar proteins, including the yeast CDC10, contains a GTP-binding motif. The yeast CDC10 protein is a structural component of the 10 nm filament which lies inside the cytoplasmic membrane and is essential for cytokinesis. This human protein functions in gliomagenesis and in the suppression of glioma cell growth, and it is required for the association of centromere-associated protein E with the kinetochore. Alternative splicing results in multiple transcript variants. Several related pseudogenes have been identified on chromosomes 5, 7, 9, 10, 11, 14, 17 and 19. |
Anti-Anti-SEPT3 Antibody antibody |
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STJ118990 | St John's Laboratory | 100 µl | EUR 332.4 |
Anti-Anti-SEPT1 antibody antibody |
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STJ119580 | St John's Laboratory | 100 µl | EUR 332.4 |
Description: This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis and the maintenance of cellular morphology. This gene encodes a protein that can form homo- and heterooligomeric filaments, and may contribute to the formation of neurofibrillary tangles in Alzheimer's disease. Alternatively spliced transcript variants have been found but the full-length nature of these variants has not been determined. [provided by RefSeq, Dec 2012] |
Anti-Anti-SEPT6 antibody antibody |
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STJ11100949 | St John's Laboratory | 100 µl | EUR 332.4 |
Description: This gene is a member of the septin family of GTPases. Members of this family are required for cytokinesis. One version of pediatric acute myeloid leukemia is the result of a reciprocal translocation between chromosomes 11 and X, with the breakpoint associated with the genes encoding the mixed-lineage leukemia and septin 2 proteins. This gene encodes four transcript variants encoding three distinct isoforms. An additional transcript variant has been identified, but its biological validity has not been determined. |
Anti-Anti-SEPT9 Antibody antibody |
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STJ111369 | St John's Laboratory | 100 µl | EUR 332.4 |
Description: This gene is a member of the septin family involved in cytokinesis and cell cycle control. This gene is a candidate for the ovarian tumor suppressor gene. Mutations in this gene cause hereditary neuralgic amyotrophy, also known as neuritis with brachial predilection. A chromosomal translocation involving this gene on chromosome 17 and the MLL gene on chromosome 11 results in acute myelomonocytic leukemia. Multiple alternatively spliced transcript variants encoding different isoforms have been described. |
Anti-Anti-SEPT4 Antibody antibody |
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STJ112276 | St John's Laboratory | 100 µl | EUR 332.4 |
Description: This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is highly expressed in brain and heart. Alternatively spliced transcript variants encoding different isoforms have been described for this gene. One of the isoforms (known as ARTS) is distinct; it is localized to the mitochondria, and has a role in apoptosis and cancer. |
Anti-Anti-SEPT7 Antibody antibody |
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STJ116214 | St John's Laboratory | 100 µl | EUR 332.4 |
Description: This gene encodes a protein that is highly similar to the CDC10 protein of Saccharomyces cerevisiae. The protein also shares similarity with Diff 6 of Drosophila and with H5 of mouse. Each of these similar proteins, including the yeast CDC10, contains a GTP-binding motif. The yeast CDC10 protein is a structural component of the 10 nm filament which lies inside the cytoplasmic membrane and is essential for cytokinesis. This human protein functions in gliomagenesis and in the suppression of glioma cell growth, and it is required for the association of centromere-associated protein E with the kinetochore. Alternative splicing results in multiple transcript variants. Several related pseudogenes have been identified on chromosomes 5, 7, 9, 10, 11, 14, 17 and 19. |
Anti-Anti-SEPT8 Antibody antibody |
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STJ117206 | St John's Laboratory | 100 µl | EUR 332.4 |
Description: This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. |
Anti-Anti-SEPT2 Antibody antibody |
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STJ25475 | St John's Laboratory | 100 µl | EUR 332.4 |
Anti-Anti-SEPT5 Antibody antibody |
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STJ25477 | St John's Laboratory | 100 µl | EUR 332.4 |
Description: This gene is a member of the septin gene family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. This gene is mapped to 22q11, the region frequently deleted in DiGeorge and velocardiofacial syndromes. A translocation involving the MLL gene and this gene has also been reported in patients with acute myeloid leukemia. Alternative splicing results in multiple transcript variants. The presence of a non-consensus polyA signal (AACAAT) in this gene also results in read-through transcription into the downstream neighboring gene (GP1BB; platelet glycoprotein Ib), whereby larger, non-coding transcripts are produced. |
Anti-Anti-SEPT8 Antibody antibody |
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STJ25479 | St John's Laboratory | 100 µl | EUR 332.4 |
Description: This gene is a member of the septin family of nucleotide binding proteins, originally described in yeast as cell division cycle regulatory proteins. Septins are highly conserved in yeast, Drosophila, and mouse, and appear to regulate cytoskeletal organization. Disruption of septin function disturbs cytokinesis and results in large multinucleate or polyploid cells. Multiple alternatively spliced transcript variants encoding different isoforms have been found for this gene. |
Ly1 Antibody Reactive (LYAR) Antibody |
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20-abx311665 | Abbexa |
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Ly1 Antibody Reactive (LYAR) Antibody |
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abx234901-100ug | Abbexa | 100 ug | EUR 661.2 |
Ly1 Antibody Reactive (LYAR) Antibody |
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20-abx324434 | Abbexa |
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Ly1 Antibody Reactive (LYAR) Antibody |
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abx033330-400ul | Abbexa | 400 ul | EUR 627.6 |
Ly1 Antibody Reactive (LYAR) Antibody |
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abx033330-80l | Abbexa | 80 µl | EUR 343.2 |
Ly1 Antibody Reactive (LYAR) Antibody |
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20-abx123734 | Abbexa |
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Ly1 Antibody Reactive (LYAR) Antibody |
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20-abx008109 | Abbexa |
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Ly1 Antibody Reactive (LYAR) Antibody |
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20-abx014333 | Abbexa |
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