CNTD2 Antikörper
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- Target Alle CNTD2 Produkte
- CNTD2 (Cyclin N-terminal Domain Containing 2 (CNTD2))
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Reaktivität
- Human
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Wirt
- Kaninchen
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Klonalität
- Polyklonal
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Konjugat
- Dieser CNTD2 Antikörper ist unkonjugiert
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Applikation
- Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Kreuzreaktivität
- Human
- Aufreinigung
- Purified by Protein A.
- Immunogen
- KLH conjugated synthetic peptide derived from human CNTD2
- Isotyp
- IgG
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anti-Cyclin N-terminal Domain Containing 2 (CNTD2) antibody
CNTD2 Reaktivität: Human ELISA, IHC Wirt: Kaninchen Polyclonal unconjugated
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- Applikationshinweise
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IHC-P 1:200-400
IF(IHC-P) 1:50-200 - Beschränkungen
- Nur für Forschungszwecke einsetzbar
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- Format
- Liquid
- Konzentration
- 1 μg/μL
- Buffer
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % Proclin300 and 50 % Glycerol.
- Konservierungsmittel
- ProClin
- Vorsichtsmaßnahmen
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Lagerung
- 4 °C,-20 °C
- Informationen zur Lagerung
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- Haltbarkeit
- 12 months
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- Target
- CNTD2 (Cyclin N-terminal Domain Containing 2 (CNTD2))
- Andere Bezeichnung
- CNTD2 (CNTD2 Produkte)
- Synonyme
- MGC145598 antikoerper, cyclin N-terminal domain containing 2 antikoerper, CNTD2 antikoerper, cntd2 antikoerper
- Hintergrund
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Synonyms: CNTD2, CNTD 2, CNTD-2, Cyclin N terminal domain containing 2, Cyclin N terminal domain containing protein 2, FLJ13265, CNTD2_HUMAN.
Background: CNTD2 (cyclin N-terminal domain containing 2) is a 155 amino acid protein that contains one cyclin N-terminal domain and is encoded by a gene that maps to human chromosome 19q13.2. Chromosome 19 consists of approximately 63 million bases and makes up over 2 % of human genomic DNA. Chromosome 19 is recognized for having the greatest gene density of the human chromosomes. It is the genetic home for a number of immunoglobulin superfamily members, including killer cell and leukocyte Ig-like receptors, various ICAMs, the CEACAM and PSG families, and Fc?receptors. Key genes for eye color and hair color also map to chromosome 19. Peutz-Jeghers syndrome, spinocerebellar ataxia type 6, the stroke disorder CADASIL, hypercholesterolemia and insulin-dependent diabetes have been linked to chromosome 19. Translocations with chromosome 19 and chromosome 14 can be seen in some lymphoproliferative disorders and typically involve the proto-oncogene Bcl-3.
- Gen-ID
- 79935
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