SCFD2 anticorps (AA 20-585)

N° du produit ABIN7871879

Cet anticorps Lapin Polyclonal détecte spécifiquement SCFD2 dans WB, ELISA, FACS et IF. Il présente une réactivité avec des échantillons de Humain et Souris.

Aperçu rapide pour SCFD2 anticorps (AA 20-585) (ABIN7871879)

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

Reactivité: Humain, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SCFD2 est non-conjugé

Application: Western Blotting (WB), ELISA, Flow Cytometry (FACS), Immunofluorescence (IF)

Détail du produit anti-SCFD2 anticorps

Épitope: AA 20-585

Fonction: SCFD2 Antibody / Sec1 family domain-containing protein 2

Purification: Antigen affinity purified

Immunogène: E. coli-derived recombinant human protein (amino acids K20-H585) was used as the immunogen for the SCFD2 antibody.

Isotype: IgG

Information d'application

Indications d'application: Optimal dilution of the SCFD2 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 SCFD2 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 SCFD2

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

Autre désignation: SCFD2

Sujet: 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 Huntingtoni 1/2s 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

UniProt: Q8WU76