C10orf88 anticorps (Cy3)
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- Antigène Tous les produits C10orf88
- C10orf88 (Chromosome 10 Open Reading Frame 88 (C10orf88))
- Reactivité
- Humain, Souris, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp C10orf88 est conjugé à/à la Cy3
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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 C10orf88
- Isotype
- IgG
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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
- C10orf88 (Chromosome 10 Open Reading Frame 88 (C10orf88))
- Autre désignation
- C10orf88 (C10orf88 Produits)
- Synonymes
- anticorps 3110040E10Rik, anticorps AI429544, anticorps chromosome 10 open reading frame 88, anticorps RIKEN cDNA 2310057M21 gene, anticorps similar to RIKEN cDNA 2310057M21, anticorps C10orf88, anticorps 2310057M21Rik, anticorps RGD1305014
- Sujet
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Synonyms: Chromosome 10 open reading frame 88, CJ088_HUMAN, Em:AC073585.5, FLJ13490, Hypothetical protein LOC80007, Uncharacterized protein C10orf88.
Background: C10orf88 is a 445 amino acid protein encoded by a gene that maps to human chromosome 10q26.13. Spanning nearly 135 million base pairs, chromosome 10 makes up approximately 4.5 % of total DNA in cells and encodes nearly 1,200 genes. Several protein-coding genes, including those that encode for chemokines, cadherins, excision repair proteins, early growth response factors (Egrs) and fibroblast growth receptors (FGFRs), are located on chromosome 10. Defects in some of the genes that map to chromosome 10 are associated with Charcot-Marie Tooth disease, Jackson-Weiss syndrome, Usher syndrome, nonsyndromatic deafness, Wolman?s syndrome, Cowden syndrome, multiple endocrine neoplasia type 2 and porphyria.
- ID gène
- 80007
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