CXorf56 anticorps (AA 120-170) (Cy3)

N° du produit ABIN1421237

Détail du produit anti-CXorf56 anticorps (Cy3)

Antigène: CXorf56 (CXORF56) (Chromosome X Open Reading Frame 56 (CXORF56))

Épitope: AA 120-170

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CXorf56 est conjugé à/à la Cy3

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 CXorf56

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 CXorf56

Antigène: CXorf56 (CXORF56) (Chromosome X Open Reading Frame 56 (CXORF56))

Autre désignation: CXorf56 (CXORF56 Produits)

Synonymes: anticorps C4HXorf56, anticorps CXorf56, anticorps c330007p06-a, anticorps cxorf56, anticorps chromosome X open reading frame 56, anticorps chromosome 4 CXorf56 homolog, anticorps chromosome X open reading frame, human CXorf56, anticorps RIKEN cDNA C330007P06 gene, anticorps chromosome X open reading frame 56 L homeolog, anticorps CXorf56, anticorps C4HXorf56, anticorps CXHXorf56, anticorps C330007P06Rik, anticorps cxorf56.L

Sujet:

Synonyms: UPF0428 protein CXorf56, CXorf56

Background: The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. The CXorf56 gene product has been provisionally designated CXorf56 pending further characterization.

ID gène: 63932

UniProt: Q9H5V9