CTTNBP2NL anticorps (AA 5-110)
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- Antigène Tous les produits CTTNBP2NL
- CTTNBP2NL (CTTNBP2 N-terminal Like (CTTNBP2NL))
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Épitope
- AA 5-110
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Reactivité
- Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp CTTNBP2NL est non-conjugé
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Application
- Western Blotting (WB), ELISA, Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunocytochemistry (ICC)
- Réactivité croisée
- Rat
- Homologie
- Human,Mouse,Cow,Pig,Horse,Chicken,Rabbit
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human CTTNBP2NL
- Isotype
- IgG
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- Indications d'application
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WB 1:300-5000
ELISA 1:500-1000
IHC-P 1:200-400
IHC-F 1:100-500
IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200
ICC 1:100-500 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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
- 4 °C,-20 °C
- Stockage commentaire
- Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.
- Date de péremption
- 12 months
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- Antigène
- CTTNBP2NL (CTTNBP2 N-terminal Like (CTTNBP2NL))
- Autre désignation
- CTTNBP2NL (CTTNBP2NL Produits)
- Synonymes
- anticorps AA552995, anticorps AA589392, anticorps AU018624, anticorps BC003236, anticorps mKIAA1433, anticorps CTTNBP2 N-terminal like, anticorps CTTNBP2NL, anticorps Cttnbp2nl
- Sujet
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Synonyms: CT2NL_HUMAN, CTTNBP2 N terminal like, CTTNBP2 N terminal like protein, CTTNBP2 N-terminal-like protein, Cttnbp2nl, DKFZp547A023, FLJ13278, KIAA1433.
Background: CTTNBP2NL is a 639 amino acid protein that is encoded by a gene that maps to human chromosome 1p13.2. 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.
- ID gène
- 55917
- UniProt
- Q9P2B4
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