CRX anticorps (C-Term)
Aperçu rapide pour CRX anticorps (C-Term) (ABIN5518821)
Antigène
Voir toutes CRX AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- AA 265-299, C-Term
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Fonction
- Anti-CORD2/CRX Antibody
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Séquence
- DSLEFKDPTG TWKFTYNPMD PLDYKDQSAW KFQIL
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Réactivité croisée (Details)
- No cross-reactivity with other proteins.
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Attributs du produit
- Anti-CORD2/CRX Antibody (ABIN5518821). Tested in WB applications. This antibody reacts with Human. This is a premium antibody that guarantees superior quality, high affinity, and strong signals with minimal background in Western blot applications.
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Purification
- Immunogen affinity purified.
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Immunogène
- A synthetic peptide corresponding to a sequence at the C-terminus of human CORD2, identical to the related mouse and rat sequences.
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Isotype
- IgG
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Indications d'application
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Western blot, 0.1-0.5 μg/mL, Human
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Commentaires
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Antibody can be supported by chemiluminescence kit ABIN921124 in WB.
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Restrictions
- For Research Use only
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Format
- Lyophilized
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Reconstitution
- Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
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Concentration
- 500 μg/mL
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Buffer
- Each vial contains 5 mg BSA, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg Sodium azide.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- 4 °C,-20 °C
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Stockage commentaire
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Store at -20°C for one year from date of receipt. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20°C for six months. Avoid repeated freeze-thaw cycles.
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- CRX (Cone-Rod Homeobox (CRX))
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Autre désignation
- CRX
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Sujet
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Synonyms: Cone-rod homeobox protein,CRX,CORD2,
Tissue Specificity: Retina.
Background: Cone-rod homeobox protein is a protein that in humans is encoded by the CRX gene. The protein encoded by this gene is a photoreceptor-specific transcription factor which plays a role in the differentiation of photoreceptor cells. This homeodomain protein is necessary for the maintenance of normal cone and rod function. Mutations in this gene are associated with photoreceptor degeneration, Leber congenital amaurosis type III and the autosomal dominant cone-rod dystrophy 2. Several alternatively spliced transcript variants of this gene have been described, but the full-length nature of some variants has not been determined.
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Poids moléculaire
- 37 kDa
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ID gène
- 1406
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UniProt
- O43186
Antigène
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