CXX1 anticorps (PE)

N° du produit ABIN6988961

L’anticorps Lapin Polyclonal anti-CXX1 a été validé pour WB et FACS. Il convient pour détecter CXX1 dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour CXX1 anticorps (PE) (ABIN6988961)

Antigène: CXX1 (FAM127A) (Family with Sequence Similarity 127, Member A (FAM127A))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CXX1 est conjugé à/à la PE

Application: Western Blotting (WB), Flow Cytometry (FACS)

Détail du produit anti-CXX1 anticorps (PE)

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human CXX1/Cerebral protein 5

Isotype: IgG

Information d'application

Indications d'application: FCM 1:20-100

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 CXX1

Antigène: CXX1 (FAM127A) (Family with Sequence Similarity 127, Member A (FAM127A))

Autre désignation: Cerebral protein 5

Sujet:

Synonyms: Mammalian retrotransposon derived protein 8C, CAAX box protein 1, Cerebral protein 5, CXX 1, FAM127A, Family with sequence similarity 127, member A, Mar8, MAR8C, Mart8, F127A_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 CXX1 gene product has been provisionally designated CXX1 pending further characterization.

ID gène: 8933