KIF1BP anticorps (AA 180-220) (Cy5)

N° du produit ABIN1422126

Cet anticorps anti-KIF1BP est un anticorps Lapin Polyclonal détectant KIF1BP dans WB et IF (p). Adapté pour Humain, Souris et Rat.

Aperçu rapide pour KIF1BP anticorps (AA 180-220) (Cy5) (ABIN1422126)

Antigène: KIF1BP (KIAA1279) (KIAA1279)

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp KIF1BP est conjugé à/à la Cy5

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

Détail du produit anti-KIF1BP anticorps (Cy5)

Épitope: AA 180-220

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human KBP

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 KIF1BP

Antigène: KIF1BP (KIAA1279) (KIAA1279)

Autre désignation: KBP

Sujet:

Synonyms: Hypothetical protein LOC26128, KBP, KBP_HUMAN, KIAA1279, K1-binding protein, TTC20, Uncharacterized protein KIAA1279.

Background: Chromosome 10 contains over 800 genes and 135 million nucleotides, making up nearly 4.5 % of the human genome. PTEN is an important tumor suppressor gene located on chromosome 10 and, when defective, causes a genetic predisposition to cancer development known as Cowden syndrome. The chromosome 10 encoded gene ERCC6 is important for DNA repair and is linked to Cockayne syndrome which is characterized by extreme photosensitivity and premature aging. Tetrahydrobiopterin deficiency and a number of syndromes involving defective skull and facial bone fusion are also linked to chromosome 10. As with most trisomies, trisomy 10 is rare and is deleterious. The KIAA1279 gene product has been provisionally designated KIAA1279 pending further characterization.

ID gène: 26128

UniProt: Q96EK5