IGSF21 anticorps (AA 90-140) (FITC)

N° du produit ABIN1401446

L’anticorps Lapin Polyclonal anti-IGSF21 a été validé pour WB et IF (p). Il convient pour détecter IGSF21 dans des échantillons de Humain, Souris et Rat.

Aperçu rapide pour IGSF21 anticorps (AA 90-140) (FITC) (ABIN1401446)

Antigène: IGSF21 (Immunoglobin Superfamily, Member 21 (IGSF21))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp IGSF21 est conjugé à/à la FITC

Application: Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))

Détail du produit anti-IGSF21 anticorps (FITC)

Épitope: AA 90-140

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human IGSF21

Isotype: IgG

Information d'application

Indications d'application: IF(IHC-P) 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 IGSF21

Antigène: IGSF21 (Immunoglobin Superfamily, Member 21 (IGSF21))

Autre désignation: IGSF21

Sujet:

Synonyms: FLJ41177, IGSF 21, Immunoglobin superfamily member 21, immunoglobulin superfamily member 21, MGC15730, RP11 121A23.1, IGS21_HUMAN, IgSF21

Background: IGSF21 is a 467 amino acid secreted protein that contains two Ig-like (immunoglobulin-like) domains and is a member of the immunoglobulin superfamily. Members of this family of proteins usually localize to the cell membrane, and may act as receptors in the immune response pathways. The gene encoding IGSF21 maps to human chromosome 1p36.13 and mouse chromosome 4 D3. Human chromosome 1 spans 260 million base pairs, contains over 3,000 genes and comprises nearly 8 % of the human genome. A large number of disease-associated genes are associated with chromosome 1, including those that are involved in familial adenomatous polyposis, Stickler syndrome, Parkinson?s disease, Gaucher disease, schizophrenia and Usher syndrome. Aberrations in chromosome 1 are found in a variety of cancers, including head and neck cancer, malignant melanoma and multiple myeloma.

ID gène: 84966

UniProt: Q96ID5