CXorf21 anticorps (AA 165-215) (HRP)

N° du produit ABIN1421254

Détail du produit anti-CXorf21 anticorps (HRP)

Antigène: CXorf21 (Chromosome X Open Reading Frame 21 (CXorf21))

Épitope: AA 165-215

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CXorf21 est conjugé à/à la HRP

Application: Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human CXorf21

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400

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.

Conseil sur la manipulation: Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.

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 CXorf21

Antigène: CXorf21 (Chromosome X Open Reading Frame 21 (CXorf21))

Autre désignation: CXorf21 (CXorf21 Produits)

Synonymes: anticorps CXorf21, anticorps chromosome X open reading frame 21, anticorps RIKEN cDNA 5430427O19 gene, anticorps chromosome X open reading frame, human CXorf21, anticorps CXorf21, anticorps 5430427O19Rik, anticorps CXHXorf21

Sujet:

Synonyms: Chromosome X open reading frame 21, FLJ11577, Hypothetical protein LOC80231, Uncharacterized protein CXorf21, CX021_HUMAN.

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 CXorf21 gene product has been provisionally designated CXorf21 pending further characterization.

ID gène: 80231

UniProt: Q9HAI6