RAX2 anticorps
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- Antigène Voir toutes RAX2 Anticorps
- RAX2 (Retina and Anterior Neural Fold Homeobox 2 (RAX2))
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Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp RAX2 est non-conjugé
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Application
- Western Blotting (WB)
- Réactivité croisée
- Humain
- Purification
- Purified by antigen-affinity chromatography.
- Immunogène
- Recombinant protein encompassing a sequence within the center region of human RAX2. The exact sequence is proprietary.
- Isotype
- IgG
- Top Product
- Discover our top product RAX2 Anticorps primaire
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- Indications d'application
- WB: 1:500-1:3000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
- Commentaires
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Positive Control: IMR32
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.86 mg/mL
- Buffer
- 0.1M Tris-Glycine ( pH 7), 20 % Glycerol, 0.01 % Thimerosal
- Agent conservateur
- Thimerosal (Merthiolate)
- Précaution d'utilisation
- This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
- Stock
- 4 °C,-20 °C
- Stockage commentaire
- Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
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- Antigène
- RAX2 (Retina and Anterior Neural Fold Homeobox 2 (RAX2))
- Autre désignation
- retina and anterior neural fold homeobox 2 (RAX2 Produits)
- Synonymes
- anticorps qrx, anticorps rx-l, anticorps armd6, anticorps raxl1, anticorps cord11, anticorps ARMD6, anticorps CORD11, anticorps QRX, anticorps RAXL1, anticorps retina and anterior neural fold homeobox 2 S homeolog, anticorps retina and anterior neural fold homeobox 2, anticorps rax2.S, anticorps RAX2
- Sujet
- Retina and anterior neural fold homeobox 2 , ARMD6 , CORD11 , QRX , RAXL1,This gene encodes a homeodomain-containing protein that plays a role in eye development. Mutation of this gene causes age-related macular degeneration type 6, an eye disorder resulting in accumulations of protein and lipid beneath the retinal pigment epithelium and within the Bruch's membrane. Defects in this gene can also cause cone-rod dystrophy type 11, a disease characterized by the initial degeneration of cone photoreceptor cells and resulting in loss of color vision and visual acuity, followed by the degeneration of rod photoreceptor cells, which progresses to night blindness and the loss of peripheral vision. [provided by RefSeq]
- Poids moléculaire
- 20 kDa
- ID gène
- 84839
- UniProt
- Q96IS3
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