VSX1 anticorps (N-Term)

N° du produit ABIN2780933

L’anticorps Lapin Polyclonal anti-VSX1 a été validé pour WB. Il convient pour détecter VSX1 dans des échantillons de Humain et Boeuf (Vache).

Aperçu rapide pour VSX1 anticorps (N-Term) (ABIN2780933)

Antigène: VSX1 (Visual System Homeobox 1 (VSX1))

Reactivité: Humain, Boeuf (Vache)

Hôte: Lapin

Clonalité: Polyclonal

Conjugué: Cet anticorp VSX1 est non-conjugé

Application: Western Blotting (WB)

Détail du produit anti-VSX1 anticorps

Épitope: N-Term

Séquence: MTGRDSLSDG RTSSRALVPG GSPRGSRPRG FAITDLLGLE AELPAPAGPG

Homologie: Cow: 79%, Human: 100%

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.

Purification: Protein A purified

Immunogène: The immunogen is a synthetic peptide directed towards the N terminal region of human VSX1

Information d'application

Indications d'application: Optimal working dilutions should be determined experimentally by the investigator.

Commentaires:

Antigen size: 239 AA

Restrictions: For Research Use only

Stockage

Format: Liquid

Concentration: Lot specific

Buffer: Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.

Agent conservateur: Sodium azide

Précaution d'utilisation: This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

Conseil sur la manipulation: Avoid repeated freeze-thaw cycles.

Stock: -20 °C

Stockage commentaire: For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.

Détails sur VSX1

Antigène: VSX1 (Visual System Homeobox 1 (VSX1))

Autre désignation: VSX1

Sujet: 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.
Alias Symbols: PPD, KTCN, PPCD, RINX, KTCN1, CAASDS
Protein Size: 239

Poids moléculaire: 25 kDa

ID gène: 30813

NCBI Accession: NM_199425, NP_955457