CXORF36 anticorps

N° du produit ABIN7073504

Détail du produit anti-CXORF36 anticorps

Antigène: CXORF36 (Chromosome X Open Reading Frame 36 (CXORF36))

Reactivité: Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CXORF36 est non-conjugé

Application: Western Blotting (WB)

Réactivité croisée: Rat

Purification: Affinity purification

Immunogène: Recombinant protein corresponding to Mouse CXorf36

Information d'application

Indications d'application: WB (M,R) 1:1000- 1:2000

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: PBS, pH 7.4, 0.02 % sodium azide

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Détails sur CXORF36

Antigène: CXORF36 (Chromosome X Open Reading Frame 36 (CXORF36))

Autre désignation: CXorf36 (CXORF36 Produits)

Synonymes: anticorps CXorf36, anticorps 4930578C19Rik, anticorps DIA1R, anticorps EPQL1862, anticorps PRO3743, anticorps bA435K1.1, anticorps CXORF36, anticorps chromosome 1 open reading frame, human CXorf36, anticorps chromosome X open reading frame 36, anticorps chromosome X open reading frame, human CXorf36, anticorps C1HXORF36, anticorps CXorf36, anticorps CXHXorf36

Sujet: 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. The CXorf36 gene product has been provisionally designated CXorf36 pending further characterization.

Poids moléculaire: 49 kDa

ID gène: 75905

NCBI Accession: NP_780437

UniProt: Q8C3I9