SIM1 anticorps (N-Term)
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- Antigène Voir toutes SIM1 Anticorps
- SIM1 (Single-Minded Homolog 1 (SIM1))
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Épitope
- AA 1-30, N-Term
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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 SIM1 est non-conjugé
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Application
- Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p))
- Homologie
- Zf, M, D
- Purification
- This antibody is purified through a protein A column, followed by peptide affinity purification.
- Immunogène
- This SIM1 antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 1-30 amino acids from the N-terminal region of human SIM1.
- Clone
- RB32160
- Isotype
- Ig Fraction
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- Indications d'application
- WB: 1:1000. WB: 1:2000. IHC-P-Leica: 1:250. IHC-P-Leica: 1:250
- Restrictions
- For Research Use only
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- Format
- Liquid
- Buffer
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) 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
- SIM1 Antibody (N-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.
- Date de péremption
- 6 months
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- Antigène
- SIM1 (Single-Minded Homolog 1 (SIM1))
- Autre désignation
- SIM1 (SIM1 Produits)
- Synonymes
- anticorps bHLHe14, anticorps mSIM1, anticorps single-minded family bHLH transcription factor 1, anticorps single-minded homolog 1 (Drosophila), anticorps single-minded family bHLH transcription factor 1a, anticorps SIM1, anticorps Sim1, anticorps sim1a
- Sujet
- SIM1 and SIM2 genes are Drosophila single-minded (sim) gene homologs. SIM1 transcript was detected only in fetal kidney out of various adult and fetal tissues tested. Since the sim gene plays an important role in Drosophila development and has peak levels of expression during the period of neurogenesis,it was proposed that the human SIM gene is a candidate for involvement in certain dysmorphic features (particularly the facial and skull characteristics), abnormalities of brain development, and/or mental retardation of Down syndrome.
- ID gène
- 6492
- NCBI Accession
- NP_005059
- UniProt
- P81133
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