CCDC93 anticorps (AA 531-631) (Biotin)

N° du produit ABIN888357

Détail du produit anti-CCDC93 anticorps (Biotin)

Antigène: CCDC93 (Coiled-Coil Domain Containing 93 (CCDC93))

Épitope: AA 531-631

Reactivité: Rat

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp CCDC93 est conjugé à/à la Biotin

Application: ELISA, Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunohistochemistry (Frozen Sections) (IHC (fro))

Réactivité croisée: Rat

Homologie: Human,Mouse,Dog,Cow,Sheep,Pig

Purification: Purified by Protein A.

Immunogène: KLH conjugated synthetic peptide derived from human CCDC93

Isotype: IgG

Information d'application

Indications d'application: IHC-P 1:200-400
IHC-F 1:100-500

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 for 12 months.

Date de péremption: 12 months

Détails sur CCDC93

Antigène: CCDC93 (Coiled-Coil Domain Containing 93 (CCDC93))

Autre désignation: CCDC93 (CCDC93 Produits)

Synonymes: anticorps 4633402D15Rik, anticorps 9230102M16Rik, anticorps coiled-coil domain containing 93, anticorps coiled-coil domain containing 93 L homeolog, anticorps CCDC93, anticorps Ccdc93, anticorps ccdc93.L

Sujet:

Synonyms: CCDC 93, Coiled-coil domain containing 93, FLJ10996, FLJ25197, MGC13033, CCD93_HUMAN.

Background: The coiled-coil domain is a structural motif found in proteins that are involved in a diverse array of biological functions such as the regulation of gene expression, cell division, membrane fusion, and drug extrusion and delivery. CCDC93 (coiled-coil domain containing 93) is a 631 amino acid protein that belongs to the CCDC93 family. CCDC93 is encoded by a gene located on human chromosome 2, which makes up approximately 8 % of the human genome and contains 237 million bases encoding over 1,400 genes. A number of genetic diseases are linked to genes on chromosome 2. Harlequin icthyosis, a rare 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, Alstr syndrome, is related to mutations in the ALMS1 gene.

ID gène: 54520