FCHSD1 anticorps (AA 151-250) (Alexa Fluor 594)

N° du produit ABIN2813187

Détail du produit anti-FCHSD1 anticorps (Alexa Fluor 594)

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

Épitope: AA 151-250

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FCHSD1 est conjugé à/à la Alexa Fluor 594

Application: Immunofluorescence (Cultured Cells) (IF (cc)), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

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: IF(IHC-P) 1:50-200
IF(IHC-F) 1:50-200
IF(ICC) 1:50-200

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 FCHSD1

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

Autre désignation: FCHSD1 (FCHSD1 Produits)

Synonymes: anticorps NWK2, anticorps A030002D08Rik, anticorps FCH and double SH3 domains 1, anticorps Fchsd1, anticorps 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