C10orf62 anticorps (Alexa Fluor 680)

N° du produit ABIN4997857

Détail du produit anti-C10orf62 anticorps (Alexa Fluor 680)

Antigène: C10orf62 (C10ORF62) (Chromosome 10 Open Reading Frame 62 (C10ORF62))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp C10orf62 est conjugé à/à la Alexa Fluor 680

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 C10orf62

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 C10orf62

Antigène: C10orf62 (C10ORF62) (Chromosome 10 Open Reading Frame 62 (C10ORF62))

Autre désignation: C10orf62 (C10ORF62 Produits)

Synonymes: anticorps bA548K23.1, anticorps chromosome 10 open reading frame 62, anticorps C10orf62

Sujet:

Synonyms: bA548K23.1, Hypothetical protein LOC414157, MERIT40, chromosome 10 open reading frame 62, NBA1, Uncharacterized protein C10orf62, CJ062_HUMAN .

Background: C10orf62 is a 223 amino acid protein encoded by a gene that maps to human chromosome 10q24.1. 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: 414157