SAYSD1 anticorps (AA 130-180)

N° du produit ABIN1385609

L’anticorps Lapin Polyclonal anti-SAYSD1 a été validé pour WB, IF (p) et IHC (p). Il convient pour détecter SAYSD1 dans des échantillons de Humain, Rat et Souris.

Aperçu rapide pour SAYSD1 anticorps (AA 130-180) (ABIN1385609)

Antigène: SAYSD1 (SAYSVFN Motif Domain Containing 1 (SAYSD1))

Reactivité: Humain, Rat, Souris

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp SAYSD1 est non-conjugé

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

Détail du produit anti-SAYSD1 anticorps

Épitope: AA 130-180

Réactivité croisée: Humain, Souris, Rat

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human C6orf64

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 SAYSD1

Antigène: SAYSD1 (SAYSVFN Motif Domain Containing 1 (SAYSD1))

Autre désignation: C6orf64

Sujet:

Synonyms: Chromosome 6 open reading frame 64, DKFZp434H012, FLJ11101, Hypothetical protein LOC55776, Uncharacterized protein C6orf64, SMDC1_HUMAN, SAYSD1, SAYSvFN domain-containing protein 1

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. The C6orf64 gene product has been provisionally designated C6orf64 pending further characterization.

ID gène: 55776

UniProt: Q9NPB0