C7orf45 anticorps (AA 51-150) (Biotin)
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- Antigène Tous les produits C7orf45 (SSMEM1)
- C7orf45 (SSMEM1) (Serine-Rich Single-Pass Membrane Protein 1 (SSMEM1))
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Épitope
- AA 51-150
- Reactivité
- Humain
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Hôte
- Lapin
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Clonalité
- Polyclonal
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Conjugué
- Cet anticorp C7orf45 est conjugé à/à la Biotin
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Application
- ELISA, Immunohistochemistry (Frozen Sections) (IHC (fro)), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Homologie
- Human,Mouse
- Purification
- Purified by Protein A.
- Immunogène
- KLH conjugated synthetic peptide derived from human C7orf45
- Isotype
- IgG
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- Indications d'application
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IHC-P 1:200-400
IHC-F 1:100-500 - Restrictions
- For Research Use only
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- Format
- Liquid
- Concentration
- 1 μg/μL
- Buffer
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
- Agent conservateur
- ProClin
- Précaution d'utilisation
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
- Stock
- -20 °C
- Stockage commentaire
- Store at -20°C for 12 months.
- Date de péremption
- 12 months
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- Antigène
- C7orf45 (SSMEM1) (Serine-Rich Single-Pass Membrane Protein 1 (SSMEM1))
- Autre désignation
- C7orf45 (SSMEM1 Produits)
- Synonymes
- anticorps C7orf45, anticorps RGD1559502, anticorps 1700016K02Rik, anticorps 1700025E21Rik, anticorps serine rich single-pass membrane protein 1, anticorps serine-rich single-pass membrane protein 1, anticorps SSMEM1, anticorps Ssmem1
- Sujet
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Synonyms: C7orf45, CG045_HUMAN, chromosome 7 open reading frame 45, FLJ40316, Uncharacterized protein C7orf45.
Background: Chromosome 7 has been linked to Osteogenesis imperfecta, Pendred syndrome, Lissencephaly, Citrullinemia and Shwachman-Diamond syndrome. The deletion of a portion of the q arm of chromosome 7 is associated with Williams-Beuren syndrome, a condition characterized by mild mental retardation, an unusual comfort and friendliness with strangers and an elfin appearance. Deletions of portions of the q arm of chromosome 7 are also seen in a number of myeloid disorders including cases of acute myelogenous leukemia and myelodysplasia. The C7orf45 gene product has been provisionally designated C7orf45 pending further characterization.
- ID gène
- 136263
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