TMEM255B anticorps (AA 196-240)

N° du produit ABIN7871709

L’anticorps anti-TMEM255B Polyclonal Lapin est utilisé pour la détection de TMEM255B dans des échantillons de Souris et Rat. Il a été validé pour ELISA, WB et IHC (p).

Aperçu rapide pour TMEM255B anticorps (AA 196-240) (ABIN7871709)

Antigène: TMEM255B (Transmembrane Protein 255B (TMEM255B))

Reactivité: Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp TMEM255B est non-conjugé

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

Détail du produit anti-TMEM255B anticorps

Épitope: AA 196-240

Fonction: Fam70b Antibody / Tmem255b

Purification: Affinity purified

Immunogène: Recombinant mouse protein (amino acids Q196-L240) was used as the immunogen for the Fam70b antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the Fam70b antibody should be determined by the researcher.

Restrictions: For Research Use only

Stockage

Format: Lyophilized

Buffer: 0.5 mg/mL if reconstituted with 0.2 mL sterile DI water

Stock: 4 °C,-20 °C

Stockage commentaire: After reconstitution, the Fam70b antibody can be stored for up to one month at 4oC. For long-term, aliquot and store at -20oC. Avoid repeated freezing and thawing.

Détails sur TMEM255B

Antigène: TMEM255B (Transmembrane Protein 255B (TMEM255B))

Autre désignation: Fam70b

Sujet: FAM70B (family with sequence similarity 70, member B) is a 326 amino acid membrane protein that belongs to the FAM70 family. The gene that encodes FAM70B maps to human chromosome 13, which contains around 114 million base pairs and encodes roughly 400 genes. Key tumor suppressor genes on chromosome 13 include the breast cancer susceptibility gene, BRCA2, and the RB1 (retinoblastoma) gene. RB1 encodes a crucial tumor suppressor protein which, when defective, leads to malignant growth in the retina and has been implicated in a variety of other cancers. The gene SLITRK1, which is associated with Tourette syndrome, is on chromosome 13. As with most chromosomes, polysomy of part or all of chromosome 13 is deleterious to development and decreases the odds of survival. Trisomy 13, also known as Patau syndrome, is quite deadly and the few who survive past one year suffer from permanent neurologic defects, difficulty eating and vulnerability to serious respiratory infections.

UniProt: Q5FW56