TMEM184B anticorps (C-Term)
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- Antigène Voir toutes TMEM184B Anticorps
- TMEM184B (Transmembrane Protein 184B (TMEM184B))
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Épitope
- C-Term
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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 TMEM184B est non-conjugé
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Application
- Western Blotting (WB), Immunofluorescence (IF), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Enzyme Immunoassay (EIA)
- Specificité
- This antibody detects TMEM184B near C-term.
- Purification
- Peptide affinity chromatography
- Immunogène
- TMEM184B antibody was raised against a 15 amino acid peptide near the carboxy terminus of human TMEM184B.
- Isotype
- IgG
- Top Product
- Discover our top product TMEM184B Anticorps primaire
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- Indications d'application
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ELISA. Western blot.
Other applications not tested.
Optimal dilutions are dependent on conditions and should be determined by the user. - Restrictions
- For Research Use only
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- Concentration
- 1.0 mg/mL
- Buffer
- PBS containing 0.02 % 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.
- Conseil sur la manipulation
- Avoid repeated freezing and thawing.
- Stock
- 4 °C/-20 °C
- Stockage commentaire
- Store undiluted at 2-8 °C for one month or (in aliquots) at -20 °C for longer.
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- Antigène
- TMEM184B (Transmembrane Protein 184B (TMEM184B))
- Autre désignation
- TMEM184B (TMEM184B Produits)
- Synonymes
- anticorps C22orf5, anticorps FM08, anticorps HS5O6A, anticorps 2610507A11, anticorps 4732495E13Rik, anticorps RGD1306591, anticorps TMEM148B, anticorps transmembrane protein 184ba, anticorps transmembrane protein 184B, anticorps transmembrane protein 184b, anticorps tmem184ba, anticorps Tsp_04618, anticorps TMEM184B, anticorps Tmem184b
- Sujet
- TMEM184B, also known as C22orf5, is a 407 amino acid multi-pass membrane protein and represents a novel gene in the activation of the MAPK signaling pathway. The gene encoding TMEM184B maps to human chromosome 22, mutations in several of the genes in chromosome 22 are involved in the development of autism, schizophrenia, Phelan-McDermid syndrome and Neurofibromatosis type 2, suggesting that TMEM184B may play a role in these syndromes.Synonyms: C22orf5, Putative MAPK-activating protein FM08, Transmembrane protein 184B
- ID gène
- 25829
- NCBI Accession
- NP_036396
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