CWF19L1 anticorps (Biotin)
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- Antigène Tous les produits CWF19L1
- CWF19L1 (CWF19-Like 1, Cell Cycle Control (CWF19L1))
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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 CWF19L1 est conjugé à/à la Biotin
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Application
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Réactivité croisée
- Humain, Souris, Rat
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human CWF19L1
- Isotype
- IgG
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- Indications d'application
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WB 1:300-5000
IHC-P 1:200-400 - 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 for 12 months.
- Date de péremption
- 12 months
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- Antigène
- CWF19L1 (CWF19-Like 1, Cell Cycle Control (CWF19L1))
- Autre désignation
- CWF19L1 (CWF19L1 Produits)
- Synonymes
- anticorps 2610528C06Rik, anticorps AI854304, anticorps AV336991, anticorps CWF19-like 1, cell cycle control (S. pombe), anticorps CWF19 like 1, cell cycle control (S. pombe), anticorps CWF19 like 1, cell cycle control (S. pombe) L homeolog, anticorps Cwf19l1, anticorps CWF19L1, anticorps cwf19l1.L
- Sujet
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Synonyms: CWF19-like 1, cell cycle control, C19L1_HUMAN.
Background: CWF19L1 is a 538 amino acid protein belonging to the CWF19 family and exists as three alternatively spliced isoforms. CWF19L1 is encoded by a gene located on human chromosome 10, which spans nearly 135 million base pairs, 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
- 55280
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