FASTKD1 anticorps

N° du produit ABIN7263405

Détail du produit anti-FASTKD1 anticorps

Antigène: FASTKD1 (FAST Kinase Domains 1 (FASTKD1))

Reactivité: Humain, Souris, Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp FASTKD1 est non-conjugé

Application: Immunohistochemistry (IHC)

Attributs du produit: Polyclonal Antibody

Purification: Affinity purification

Immunogène: Recombinant fusion protein of human FASTKD1 (NP_078898.3).

Isotype: IgG

Information d'application

Indications d'application: IHC 1:50-1:200

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: 1 mg/mL

Buffer: PBS with 0.02 % sodium azide, 50 % glycerol, pH 7.3

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. Avoid freeze / thaw cycles.

Détails sur FASTKD1

Antigène: FASTKD1 (FAST Kinase Domains 1 (FASTKD1))

Autre désignation: FASTKD1 (FASTKD1 Produits)

Synonymes: anticorps zgc:77397, anticorps fakd1, anticorps 5330408N05Rik, anticorps mKIAA1800, anticorps RGD1563531, anticorps FAST kinase domains 1, anticorps FAST kinase domain-containing protein 1, anticorps FAST kinase domains 1 L homeolog, anticorps fastkd1, anticorps fakd1, anticorps FASTKD1, anticorps Fastkd1, anticorps fastkd1.L

Sujet: The second largest human chromosome, 2 consists of 237 million bases encoding over 1,400 genes and making up approximately 8 % of the human genome. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare and morbid skin deformity, is associated with mutations in the ABCA12 gene. The lipid metabolic disorder sitosterolemia is associated with ABCG5 and ABCG8. An extremely rare recessive genetic disorder, Alstrm syndrome is due to mutations in the ALMS1 gene. Interestingly, chromosome 2 contains what appears to be a vestigial second centromere and vestigial telomeres which gives credence to the hypothesis that human chromosome 2 is the result of an ancient fusion of two ancestral chromosomes seen in modern form today in apes.

ID gène: 79675

UniProt: Q53R41