TMEM132E anticorps (C-Term)
Cet anticorps anti-TMEM132E est un anticorps Lapin Polyclonal détectant TMEM132E dans WB et FACS. Adapté pour Souris et Humain. Ce Primary Antibody a été cité dans 1 publication.
(1 reference)
N° du produit ABIN655434
Aperçu rapide pour TMEM132E anticorps (C-Term) (ABIN655434)
Antigène
Voir toutes TMEM132E Anticorps
TMEM132E
(Transmembrane Protein 132E (TMEM132E))
Reactivité
Souris, Humain
Hôte
Lapin
Clonalité
Polyclonal
Conjugué
Cet anticorp TMEM132E est non-conjugé
Application
Western Blotting (WB), Flow Cytometry (FACS)
Clone
RB29313
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Épitope
- AA 704-733, C-Term
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Purification
- This antibody is purified through a protein A column, followed by peptide affinity purification.
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Immunogène
- This TMEM132E antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 704-733 amino acids from the C-terminal region of human TMEM132E.
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Isotype
- Ig Fraction
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anti-Transmembrane Protein 132E (TMEM132E) antibody
TMEM132E Reactivité: Souris, Rat WB Hôte: Lapin Polyclonal unconjugated
anti-Transmembrane Protein 132E (TMEM132E) antibodyTMEM132E Reactivité: Souris WB Hôte: Lapin Polyclonal unconjugated
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Indications d'application
- WB: 1:1000. WB: 1:1000. FC: 1:10~50
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Restrictions
- For Research Use only
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Format
- Liquid
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Buffer
- Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
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Agent conservateur
- Sodium azide
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Précaution d'utilisation
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Stock
- 4 °C,-20 °C
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Stockage commentaire
- Maintain refrigerated at 2-8 °C for up to 6 months. For long term storage store at -20 °C in small aliquots to prevent freeze-thaw cycles.
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Date de péremption
- 6 months
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: "Whole-exome sequencing identifies a variant in TMEM132E causing autosomal-recessive nonsyndromic hearing loss DFNB99." dans: Human mutation, Vol. 36, Issue 1, pp. 98-105, (2015) (PubMed).
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: "Whole-exome sequencing identifies a variant in TMEM132E causing autosomal-recessive nonsyndromic hearing loss DFNB99." dans: Human mutation, Vol. 36, Issue 1, pp. 98-105, (2015) (PubMed).
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