CXorf21 anticorps (AA 165-215)

N° du produit ABIN1385430

Cet anticorps anti-CXorf21 Polyclonal Lapin (ABIN1385430) détecte spécifiquement CXorf21 dans FACS, IF (p) et IHC (p). L’anticorps est réactif avec des échantillons de Humain.

Aperçu rapide pour CXorf21 anticorps (AA 165-215) (ABIN1385430)

Antigène: CXorf21 (TASL) (TLR Adaptor Interacting With Endolysosomal SLC15A4 (TASL))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CXorf21 est non-conjugé

Application: Flow Cytometry (FACS), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-CXorf21 anticorps

Épitope: AA 165-215

Fonction: CXorf21 Polyclonal Antibody

Réactivité croisée: Humain

Homologie: Mouse,Rat,Dog,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human CXorf21

Isotype: IgG

Information d'application

Indications d'application: FCM(1:300-5000), IHC-P(1:200-400), IF(IHC-P)(1:50-200)

Restrictions: For Research Use only

Stockage

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 4C. Store at -20C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur CXorf21

Antigène: CXorf21 (TASL) (TLR Adaptor Interacting With Endolysosomal SLC15A4 (TASL))

Autre désignation: CXorf21

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