ZC2HC1C anticorps (Cy5.5)

N° du produit ABIN1421527

Détail du produit anti-ZC2HC1C anticorps (Cy5.5)

Antigène: ZC2HC1C (Zinc Finger, C2HC-Type Containing 1C (ZC2HC1C))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp ZC2HC1C est conjugé à/à la Cy5.5

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 C14ORF140/FAM164C

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Stockage

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

Détails sur ZC2HC1C

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:

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.