TEX261 anticorps (AA 121-196)

N° du produit ABIN1386683

L’anticorps anti-TEX261 Polyclonal Lapin est utilisé pour la détection de TEX261 dans des échantillons de Humain. Il a été validé pour IHC (p), IF (cc), IF (p) et IHC (fro).

Aperçu rapide pour TEX261 anticorps (AA 121-196) (ABIN1386683)

Antigène: TEX261 (Testis Expressed 261 (TEX261))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TEX261 est non-conjugé

Application: Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Détail du produit anti-TEX261 anticorps

Épitope: AA 121-196

Fonction: TEX261 Polyclonal Antibody

Homologie: Human,Dog,Cow,Sheep,Pig,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human TEX261

Isotype: IgG

Information d'application

Indications d'application: Optimal working dilution should be determined by the investigator.

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 TEX261

Antigène: TEX261 (Testis Expressed 261 (TEX261))

Autre désignation: TEX261

Sujet:

Synonyms: 3110001O07Rik, AA409339, AI480706, AL033351, Protein TEX261, TEG 261, TEX261, TX261_HUMAN, UNQ1882/PRO4325.

Background: TEX261 is a 196 amino acid multi-pass membrane protein that belongs to the SVP26 family. The gene that encodes TEX261 consists of approximately 47,406 bases and maps to human chromosome 2p13.3. Consisting of 237 million bases, Chromosome 2 encodes over 1,400 genes and makes up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstr syndrome, is due to mutations in the ALMS1 gene.