CXorf21 anticorps (AA 165-215) (AbBy Fluor® 488)
-
- Antigène Tous les produits CXorf21
- CXorf21 (Chromosome X Open Reading Frame 21 (CXorf21))
-
Épitope
- AA 165-215
- Reactivité
- Humain, Souris, Rat
-
Hôte
- Lapin
-
Clonalité
- Polyclonal
-
Conjugué
- Cet anticorp CXorf21 est conjugé à/à la AbBy Fluor® 488
-
Application
- Western Blotting (WB), Flow Cytometry (FACS), Immunofluorescence (Paraffin-embedded Sections) (IF (p))
- Réactivité croisée
- Humain, Souris, Rat
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human CXorf21
- Isotype
- IgG
-
-
- Indications d'application
-
FCM 1:20-100
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
- CXorf21 (Chromosome X Open Reading Frame 21 (CXorf21))
- Autre désignation
- CXorf21 (CXorf21 Produits)
- Synonymes
- anticorps CXorf21, anticorps chromosome X open reading frame 21, anticorps RIKEN cDNA 5430427O19 gene, anticorps chromosome X open reading frame, human CXorf21, anticorps CXorf21, anticorps 5430427O19Rik, anticorps CXHXorf21
- Sujet
-
Synonyms: Chromosome X open reading frame 21, FLJ11577, Hypothetical protein LOC80231, Uncharacterized protein CXorf21, CX021_HUMAN.
Background: The X and Y chromosomes are the human sex chromosomes. Chromosome X consists of about 153 million base pairs and nearly 1,000 genes. The combination of an X and Y chromosome lead to normal male development while two copies of X lead to normal female development. There are a number of conditions related to an unsual number and combination of sex chromosomes being inherited. More than one copy of the X chromosome with a Y chromosome causes Klinefelter's syndrome. A single copy of X alone leads to Turner's syndrome. More than 2 copies of the X chromosome, in the absence of a Y chromosome, is known as Triple X syndrome. Color blindness, hemophilia, and Duchenne muscular dystrophy are well known X chromosome-linked conditions which affect males more frequently as males carry a single X chromosome. The CXorf21 gene product has been provisionally designated CXorf21 pending further characterization.
- ID gène
- 80231
- UniProt
- Q9HAI6
-