TMEM199 anticorps (AA 20-129)
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- Antigène Tous les produits TMEM199
- TMEM199 (Transmembrane Protein 199 (TMEM199))
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Épitope
- AA 20-129
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Reactivité
- Humain, Souris, Rat
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp TMEM199 est non-conjugé
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Application
- Western Blotting (WB), ELISA
- Fonction
- Rabbit IgG polyclonal antibody for TMEM199 detection. Tested with WB, Direct ELISA in Human,Mouse,Rat.
- Réactivité croisée (Details)
- No cross reactivity with other proteins.
- Attributs du produit
- Rabbit IgG polyclonal antibody for TMEM199 detection. Tested with WB, Direct ELISA in Human,Mouse,Rat.
- Purification
- Immunogen affinity purified.
- Immunogène
- E.coli-derived human TMEM199 recombinant protein (Position: E20-H129).
- Isotype
- IgG
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- Indications d'application
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Application details: Western blot|0.1-0.5 μg/mL Direct ELISA|0.1-0.5 μg/mL
- Commentaires
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Tested Species: In-house tested species with positive results. Other applications have not been tested. Optimal dilutions should be determined by end users.
- Restrictions
- For Research Use only
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- Format
- Lyophilized
- Reconstitution
- Add 0.2 mL of distilled water will yield a concentration of 500 μg/mL.
- Buffer
- Each vial contains 4 mg Trehalose, 0.9 mg NaCl, 0.2 mg Na2HPO4, 0.05 mg Sodium azide.
- 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.
- Stock
- 4 °C,-20 °C
- Stockage commentaire
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At -20°C for one year. After reconstitution, at 4°C for one month.
It can also be aliquotted and stored frozen at -20 °C for a longer time. Avoid repeated freezing and thawing.
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- Antigène
- TMEM199 (Transmembrane Protein 199 (TMEM199))
- Autre désignation
- TMEM199 (TMEM199 Produits)
- Synonymes
- anticorps C17orf32, anticorps AI316787, anticorps AI848469, anticorps R74819, anticorps transmembrane protein 199, anticorps TMEM199, anticorps Tmem199
- Sujet
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Synonyms: Transmembrane protein 199, TMEM199, C17orf32
Background: TMEM199 encodes a protein homologous to the yeast V-ATPase assembly factor Vma12 and appears to be involved in Golgi homeostasis. The protein encoded by this gene has been observed to localize to the endoplasmic reticulum (ER)-Golgi intermediate compartment (ERGIC) and coat protein complex I (COPI) in some human cells. Defects in this gene are a cause of congenital disorder of glycosylation, type IIp. By genomic sequence analysis, the TMEM199 gene is mapped to chromosome 17q11.1.
- ID gène
- 147007
- UniProt
- Q8N511
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