CXorf56 anticorps (AA 120-170) (Biotin)
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- Antigène Voir toutes CXorf56 (CXORF56) Anticorps
- CXorf56 (CXORF56) (Chromosome X Open Reading Frame 56 (CXORF56))
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Épitope
- AA 120-170
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Reactivité
- Humain, Souris, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp CXorf56 est conjugé à/à la Biotin
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Application
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Réactivité croisée
- Humain, Souris, Rat
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human CXorf56
- Isotype
- IgG
- Top Product
- Discover our top product CXORF56 Anticorps primaire
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- Indications d'application
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WB 1:300-5000
IHC-P 1:200-400 - Restrictions
- For Research Use only
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- 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
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- Antigène
- CXorf56 (CXORF56) (Chromosome X Open Reading Frame 56 (CXORF56))
- Autre désignation
- CXorf56 (CXORF56 Produits)
- Synonymes
- anticorps C4HXorf56, anticorps CXorf56, anticorps c330007p06-a, anticorps cxorf56, anticorps chromosome X open reading frame 56, anticorps chromosome 4 CXorf56 homolog, anticorps chromosome X open reading frame, human CXorf56, anticorps RIKEN cDNA C330007P06 gene, anticorps chromosome X open reading frame 56 L homeolog, anticorps CXorf56, anticorps C4HXorf56, anticorps CXHXorf56, anticorps C330007P06Rik, anticorps cxorf56.L
- Sujet
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Synonyms: UPF0428 protein CXorf56, CXorf56
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 CXorf56 gene product has been provisionally designated CXorf56 pending further characterization.
- ID gène
- 63932
- UniProt
- Q9H5V9
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