DPCR1 anticorps (PE)

N° du produit ABIN1434232

Cet anticorps Lapin Polyclonal détecte spécifiquement DPCR1 dans WB. Il présente une réactivité envers Humain.

Aperçu rapide pour DPCR1 anticorps (PE) (ABIN1434232)

Antigène: DPCR1 (Diffuse Panbronchiolitis Critical Region 1 (DPCR1))

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DPCR1 est conjugé à/à la PE

Application: Western Blotting (WB)

Détail du produit anti-DPCR1 anticorps (PE)

Réactivité croisée: Humain

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human DPCR1

Isotype: IgG

Information d'application

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: 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: Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.

Date de péremption: 12 months

Détails sur DPCR1

Antigène: DPCR1 (Diffuse Panbronchiolitis Critical Region 1 (DPCR1))

Autre désignation: DPCR1

Sujet:

Synonyms: Dfuse panbronchiolitis critical region 1, Dfuse panbronchiolitis critical region, Dfuse panbronchiolitis critical region protein 1, DKFZp666O235, DPCR protein, MGC126710, MGC126712, OTTHUMP00000062447, PBLT, bCX105N19.6, DPCR1_HUMAN.

Background: Making up nearly 6 % of the human genome, chromosome 6 contains around 1,200 genes within 170 million base pairs of sequence. Deletion of a portion of the q arm of chromosome 6 is associated with early onset intestinal cancer, suggesting the presence of a cancer susceptibility locus. Porphyria cutanea tarda is associated with chromosome 6 through the HFE gene which, when mutated, predisposes an individual to developing this porphyria. Notably, the PARK2 gene, which is associated with Parkinson's disease, and the genes encoding the major histocompatiblity complex proteins, which are key molecular components of the immune system and determine predisposition to rheumatic diseases, are also located on chromosome 6. Stickler syndrome, 21-hydroxylase deficiency and maple syrup urine disease are also associated with genes on chromosome 6. A bipolar disorder susceptibility locus has been identified on the q arm of chromosome 6.

Poids moléculaire: 56kDa

ID gène: 135656