TCEANC2 anticorps (AbBy Fluor® 680)
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- Antigène Voir toutes TCEANC2 Anticorps
- TCEANC2 (Transcription Elongation Factor A (SII) N-Terminal and Central Domain Containing 2 (TCEANC2))
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Reactivité
- Humain, Rat, Souris
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp TCEANC2 est conjugé à/à la AbBy Fluor® 680
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Application
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Réactivité croisée
- Humain, Souris, Rat
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human C1orf83
- Isotype
- IgG
- Top Product
- Discover our top product TCEANC2 Anticorps primaire
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- Indications d'application
- IF(IHC-P) 1:50-200
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Agent conservateur
- ProClin
- Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Date de péremption
- 12 months
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- Antigène
- TCEANC2 (Transcription Elongation Factor A (SII) N-Terminal and Central Domain Containing 2 (TCEANC2))
- Autre désignation
- C1orf83 (TCEANC2 Produits)
- Synonymes
- anticorps C1orf83, anticorps RP4-758J24.3, anticorps 2210010B22Rik, anticorps 2210012G02Rik, anticorps 6330404A07Rik, anticorps AU015593, anticorps Tdeanc2, anticorps si:dkey-63k7.9, anticorps tcean2, anticorps transcription elongation factor A N-terminal and central domain containing 2, anticorps transcription elongation factor A (SII) N-terminal and central domain containing 2, anticorps TCEANC2, anticorps Tceanc2, anticorps tceanc2
- Sujet
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Synonyms: chromosome 1 open reading frame 83, FLJ32112, FLJ39169, hypothetical protein LOC127428, Uncharacterized protein C1orf83, TEAN2_HUMAN.
Background: Chromosome 1 is the largest human chromosome spanning about 260 million base pairs and making up 8 % of the human genome. There are about 3,000 genes on chromosome 1, and considering the great number of genes there are also a large number of diseases associated with chromosome 1. Notably, the rare aging disease Hutchinson-Gilford progeria is associated with the LMNA gene which encodes lamin A. When defective, the LMNA gene product can build up in the nucleus and cause characteristic nuclear blebs. The mechanism of rapidly enhanced aging is unclear and is a topic of continuing exploration. The MUTYH gene is located on chromosome 1 and is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome are also associated with chromosome 1. A breakpoint has been identified in 1q which disrupts the DISC1 gene and is linked to schizophrenia. Aberrations in chromosome 1 are found in a variety of cancers including head and neck cancer, malignant melanoma and multiple myeloma. The C1orf83 gene product has been provisionally designated C1orf83 pending further characterization. There are two isoforms of C1orf83 that are produced as a result of alternative splicing events.
- ID gène
- 127428
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