FCHSD1 anticorps (AA 151-250)

N° du produit ABIN1387421

L’anticorps anti-FCHSD1 Polyclonal Lapin est utilisé pour la détection de FCHSD1 dans des échantillons de Humain. Il a été validé pour IF (cc), IF (p), IHC (p) et IHC (fro).

Aperçu rapide pour FCHSD1 anticorps (AA 151-250) (ABIN1387421)

Antigène: FCHSD1 (Similar To FCH and Double SH3 Domains 1 (FCHSD1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FCHSD1 est non-conjugé

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

Détail du produit anti-FCHSD1 anticorps

Épitope: AA 151-250

Fonction: FCHSD1 Polyclonal Antibody

Réactivité croisée: Humain, Souris

Homologie: Rat,Dog,Cow,Horse,Rabbit

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human FCHSD1

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 FCHSD1

Antigène: FCHSD1 (Similar To FCH and Double SH3 Domains 1 (FCHSD1))

Autre désignation: FCHSD1

Sujet:

Synonyms: FCH and double SH3 domains 1, FCH and double SH3 domains protein 1, FCHSD 1, FCHSD1, FCSD1_HUMAN, FLJ00007, Nervous wreck homolog 2, NWK 2, NWK2.

Background: FCHSD1 is a 690 amino acid protein that contains one FCH domain and two SH3 domains. FCHSD1 exists as three isoforms as a result of alternative splicing events. The gene encoding FCHSD1 maps to chromosome 5, which is associated with Cockayne syndrome through the ERCC8 gene and familial adenomatous polyposis through the adenomatous polyposis coli (APC) tumor suppressor gene. Treacher Collins syndrome is also chromosome 5 associated and is caused by insertions or deletions within the TCOF1 gene. Deletion of the p arm of chromosome 5 leads to Cri du chat syndrome. Deletion of 5q or chromosome 5 altogether is common in therapy-related acute myelogenous leukemias and myelodysplastic syndrome.

ID gène: 89848