VSX1 anticorps (Middle Region)
Aperçu rapide pour VSX1 anticorps (Middle Region) (ABIN2776514)
Antigène
Voir toutes VSX1 AnticorpsReactivité
Hôte
Clonalité
Conjugué
Application
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Épitope
- Middle Region
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Fonction
- VSX1 Antibody - middle region
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Séquence
- FLPPRGPEPA APLAPSRPPP ALGRQKRSDS VSTSDEDSQS EDRNDLKASP
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Homologie
- Cow: 93%, Dog: 86%, Horse: 93%, Human: 100%, Mouse: 79%, Pig: 86%, Yeast: 86%
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Attributs du produit
- This is a rabbit polyclonal antibody against VSX1. It was validated on Western Blot using a cell lysate as a positive control.
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Purification
- Affinity Purified
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Immunogène
- The immunogen is a synthetic peptide directed towards the middle region of human VSX1
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Indications d'application
- Optimal working dilution should be determined by the investigator.
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Commentaires
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We also sell a specific blocking peptide that can be used in combination with this antibody. You can find the blocking peptide under AAP35883-100UG
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Restrictions
- For Research Use only
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Format
- Liquid
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Concentration
- 0.5 mg/mL
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Buffer
- Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
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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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Conseil sur la manipulation
- prevent freeze-thaw cycles
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Stock
- 4 °C,-20 °C
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Stockage commentaire
- For short term use, store at 2-8C up to 1 week. For long term storage, store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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- VSX1 (Visual System Homeobox 1 (VSX1))
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Autre désignation
- VSX1
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Sujet
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Background Information: VSX1 contains a paired-like homeodomain and binds to the core of the locus control region of the red/green visual pigment gene cluster. VSX1 may regulate expression of the cone opsin genes early in development. Mutations in this gene can cause posterior polymorphous corneal dystrophy (PPCD) and keratoconus. The protein encoded by this gene contains a paired-like homeodomain and binds to the core of the locus control region of the red/green visual pigment gene cluster. The encoded protein may regulate expression of the cone opsin genes early in development. Mutations in this gene can cause posterior polymorphous corneal dystrophy (PPCD) and keratoconus. Two transcript variants encoding different isoforms have been found for this gene. The protein encoded by this gene contains a paired-like homeodomain and binds to the core of the locus control region of the red/green visual pigment gene cluster. The encoded protein may regulate expression of the cone opsin genes early in development. Mutations in this gene can cause posterior polymorphous corneal dystrophy and keratoconus. Alternatively spliced transcript variants encoding different isoforms have been described.
Gene Name: Visual system homeobox 1
Alternative Symbols: PPD, KTCN, PPCD, RINX, KTCN1, PPCD1, CAASDS
Protein Name: Visual system homeobox 1
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Poids moléculaire
- 38kDa
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ID gène
- 30813
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NCBI Accession
- NP_055403
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UniProt
- Q9NZR4
Antigène
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