SCFD2 anticorps (AA 501-600) (HRP)

N° du produit ABIN6944826

Cet anticorps Lapin Polyclonal détecte spécifiquement SCFD2 dans WB, ELISA, IHC (fro) et IHC (p). Il présente une réactivité envers Humain, Souris et Rat.

Aperçu rapide pour SCFD2 anticorps (AA 501-600) (HRP) (ABIN6944826)

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

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

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

Application: Western Blotting (WB), ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))

Détail du produit anti-SCFD2 anticorps (HRP)

Épitope: AA 501-600

Réactivité croisée: Humain, Souris, Rat

Homologie: Dog,Cow,Sheep,Pig,Horse

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human SCFD2

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500

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 SCFD2

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

Autre désignation: SCFD2

Sujet:

Synonyms: FLJ21060, FLJ39514, SCFD 2, Scfd2, SCFD2_HUMAN, Sec1 family domain containing 2, Sec1 family domain containing protein 2, Sec1 family domain-containing protein 2, STXBP1L1, Syntaxin binding protein 1 like 1, Syntaxin-binding protein 1-like 1.

Background: SCFD2 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.

ID gène: 152579

UniProt: Q8WU76