SCFD2 anticorps (AA 20-585) (APC)

N° du produit ABIN8034874

Cet anticorps anti-SCFD2 Polyclonal Lapin conjugué à APC (ABIN8034874) détecte spécifiquement SCFD2 dans FACS. L’anticorps est réactif avec des échantillons de Humain et Souris.

Aperçu rapide pour SCFD2 anticorps (AA 20-585) (APC) (ABIN8034874)

Antigène: SCFD2 (Sec1 Family Domain Containing 2 (SCFD2))

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SCFD2 est conjugé à/à la APC

Application: Flow Cytometry (FACS)

Détail du produit anti-SCFD2 anticorps (APC)

Épitope: AA 20-585

Fonction: Anti-SCFD2 Antibody APC Conjugated

Réactivité croisée (Details): No cross-reactivity with other proteins.

Purification: Immunogen affinity purified.

Immunogène: E.coli-derived human SCFD2 recombinant protein (Position: K20-H585).

Isotype: IgG

Information d'application

Indications d'application: Flow Cytometry, Optimal dilutions should be determined by end users.

Restrictions: For Research Use only

Stockage

Format: Liquid

Buffer: Each vial contains 50 % glycerol, 0.9 % NaCl, 0.2 % Na2HPO4, 0.02 % Sodium azide.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Stock: -20 °C

Stockage commentaire: At -20°C for one year from date of receipt. Avoid repeated freezing and thawing. Protect from light.

Date de péremption: 12 months

Détails sur SCFD2

Antigène: SCFD2 (Sec1 Family Domain Containing 2 (SCFD2))

Autre désignation: SCFD2

Sujet:

Background: SCFD2 (sec1 family domain containing 2), also known as STXBP1L1 (syntaxinbinding protein 1-like 1), is a 684 amino acid protein suggested to play a role in protein transport. Existing as two alternatively spliced isoforms, SCFD2 is a member of the STXBP/unc-18/SEC1 family and is encoded by a gene that maps to human chromosome 4q12. Chromosome 4 represents approximately 6 % of the human genome and contains nearly 900 genes. Notably, the Huntingtin gene, which is found to encode an expanded glutamine tract in cases of Huntington's disease, is on chromosome 4. FGFR-3 is also encoded on chromosome 4 and has been associated with thanatophoric dwarfism, achondroplasia, Muenke syndrome and bladder cancer. Chromosome 4 is also tied to Ellis-van Creveld syndrome, methylmalonic acidemia and polycystic kidney disease

Gene Full Name: sec1 family domain containing 2

ID gène: 152579

UniProt: Q8WU76