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

Produktnummer ABIN2813187

Produktdetails anti-FCHSD1 Antikörper

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

Bindungsspezifität: AA 151-250

Reaktivität: Human, Maus

Wirt: Kaninchen

Klonalität: Polyklonal

Konjugat: Dieser FCHSD1 Antikörper ist konjugiert mit Alexa Fluor 594

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

Homologie: Rat,Dog,Cow,Horse,Rabbit

Aufreinigung: Purified by Protein A.

Immunogen: KLH conjugated synthetic peptide derived from human FCHSD1

Isotyp: IgG

Anwendungsinformationen

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

Beschränkungen: Nur für Forschungszwecke einsetzbar

Handhabung

Format: Liquid

Konzentration: 1 μg/μL

Buffer: Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.

Vorsichtsmaßnahmen: This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.

Lagerung: -20 °C/-80 °C

Informationen zur Lagerung: Store at -20°C, for long storage, store at -80°C. Avoid multiple freeze-thaw cycles

Haltbarkeit: 12 months

Details zu FCHSD1

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

Andere Bezeichnung: FCHSD1 (FCHSD1 Produkte)

Synonyme: NWK2 antikoerper, A030002D08Rik antikoerper, FCH and double SH3 domains 1 antikoerper, Fchsd1 antikoerper, FCHSD1 antikoerper

Hintergrund:

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.

Subcellular location: Cytoplasm

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.

Gen-ID: 89848