DENND2C anticorps (AbBy Fluor® 750)
-
- Antigène Tous les produits DENND2C
- DENND2C (DENN/MADD Domain Containing 2C (DENND2C))
-
Reactivité
- Humain, Souris
-
Hôte
- Lapin
-
Clonalité
- Polyclonal
-
Conjugué
- Cet anticorp DENND2C est conjugé à/à la AbBy Fluor® 750
-
Application
- Western Blotting (WB), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Réactivité croisée
- Humain, Souris
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human DENND2C
- Isotype
- IgG
-
-
- Indications d'application
- IF(IHC-P) 1:50-200
- Restrictions
- For Research Use only
-
- 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. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
- Date de péremption
- 12 months
-
- Antigène
- DENND2C (DENN/MADD Domain Containing 2C (DENND2C))
- Autre désignation
- DENND2C (DENND2C Produits)
- Synonymes
- anticorps si:dkeyp-46c9.6, anticorps MGC145874, anticorps dJ1156J9.1, anticorps A930010I20Rik, anticorps RGD1308197, anticorps DENN domain containing 2C, anticorps DENN/MADD domain containing 2C, anticorps DENND2C, anticorps dennd2c, anticorps Dennd2c
- Sujet
-
Synonyms: DENN/MADD domain containing 2C, dJ1156J9.1, DKFZp686G0351, DKFZp686N1631, DKFZp779P1149, FLJ37099, RP5-1156J9.1, DEN2C_HUMAN.
Background: DENND2C is a 928 amino acid protein that contains a dDENN domain, a DENN domain, and a uDENN domain and exists as three isoforms as a result of alternative splicing. The DENND2C protein is thought to target to actin filaments and control Rab9-dependent trafficking of mannose-6-phosphate receptor to lysosomes. The gene encoding DENND2C maps to human chromosome 1, the largest human chromosome which spans about 260 million base pairs and makes up 8 % of the human genome. Other notable genes located on chromosome 1 include LMNA, which is associated with the rare aging disease Hutchinson-Gilford progeria, and the MUTYH gene, which is partially responsible for familial adenomatous polyposis. Stickler syndrome, Parkinsons, Gaucher disease and Usher syndrome.
- ID gène
- 163259
-