DPCR1 anticorps

N° du produit ABIN1386908

Détail du produit anti-DPCR1 anticorps

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

Reactivité: Humain

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp DPCR1 est non-conjugé

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

Réactivité croisée: Humain

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human DPCR1

Isotype: IgG

Information d'application

Indications d'application: WB 1:300-5000
IHC-P 1:200-400
IF(IHC-P) 1:50-200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 μg/μL

Buffer: 0.01M TBS( pH 7.4) with 1 % BSA, 0.02 % 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: 4 °C,-20 °C

Stockage commentaire: Shipped at 4°C. Store at -20°C for one year. Avoid repeated freeze/thaw cycles.

Date de péremption: 12 months

Détails sur DPCR1

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

Autre désignation: DPCR1 (DPCR1 Produits)

Synonymes: anticorps PBLT, anticorps Gm630, anticorps diffuse panbronchiolitis critical region 1, anticorps diffuse panbronchiolitis critical region 1 (human), anticorps DPCR1, anticorps 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.

ID gène: 135656