ZC2HC1C anticorps
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- Antigène Tous les produits ZC2HC1C
- ZC2HC1C (Zinc Finger, C2HC-Type Containing 1C (ZC2HC1C))
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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 ZC2HC1C est non-conjugé
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Application
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Réactivité croisée
- Humain, Souris, Rat
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human C14ORF140/FAM164C
- Isotype
- IgG
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- Indications d'application
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WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200 - 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
- ZC2HC1C (Zinc Finger, C2HC-Type Containing 1C (ZC2HC1C))
- Autre désignation
- C14ORF140 (ZC2HC1C Produits)
- Synonymes
- anticorps C14orf140, anticorps FAM164C, anticorps 2810002I04Rik, anticorps AV046379, anticorps Fam164c, anticorps RGD1307122, anticorps zinc finger C2HC-type containing 1C, anticorps zinc finger, C2HC-type containing 1C, anticorps ZC2HC1C, anticorps Zc2hc1c
- Sujet
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Synonyms: chromosome 14 open reading frame 140, FAM164C, family with sequence similarity 164 member C, FLJ23093, UPF0418 protein FAM164C, ZC21C_HUMAN.
Background: Chromosome 14 contains about 700 genes and 106 million base pairs and makes up about 3.5 % of human cellular DNA. Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease. The SERPINA1 gene is located on chromosome 14 and when defective leads to the genetic disorder ?-antitrypsin deficiency. This disorder is characterized by severe lung complications and liver dysfunction. Notably, the immunoglobulin heavy chain locus is found on chromosome 14 and has been identified as a fusion with the chromosome 19 encoded protein BCL3 in the (14,19) translocations found in a variety of B cell malignancies. The C14orf140 gene product has been provisionally designated C14orf140 pending further characterization.
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