MKS1 anticorps
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- Antigène Voir toutes MKS1 Anticorps
- MKS1 (Meckel Syndrome, Type 1 (MKS1))
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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 MKS1 est non-conjugé
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Application
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Réactivité croisée
- Humain, Rat
- Purification
- Purified by antigen-affinity chromatography.
- Immunogène
- Recombinant protein encompassing a sequence within the center region of human MKS1. The exact sequence is proprietary.
- Isotype
- IgG
- Top Product
- Discover our top product MKS1 Anticorps primaire
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- Indications d'application
- WB: 1:500-1:3000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.
- Commentaires
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Positive Control: Jurkat
- Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 0.63 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
- MKS1 (Meckel Syndrome, Type 1 (MKS1))
- Autre désignation
- MKS1 (MKS1 Produits)
- Synonymes
- anticorps BBS13, anticorps MES, anticorps MKS, anticorps POC12, anticorps AK190930, anticorps B8d3, anticorps Meckel syndrome, type 1, anticorps MKS1, anticorps Mks1
- Sujet
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Synonyms: MKS transition zone complex subunit 1 , BBS13 , JBTS28 , MES , MKS , POC12
Background: The protein encoded by this gene localizes to the basal body and is required for formation of the primary cilium in ciliated epithelial cells. Mutations in this gene result in Meckel syndrome type 1 and in Bardet-Biedl syndrome type 13. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq]
- Poids moléculaire
- 65 kDa
- ID gène
- 54903
- UniProt
- Q9NXB0
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