TMEM132E antibody (C-Term)
This anti-TMEM132E antibody is a Rabbit Polyclonal antibody detecting TMEM132E in WB and FACS. Suitable for Mouse and Human. This Primary Antibody has been cited in 1 publication.
(1 reference)
Catalog No. ABIN655434
Quick Overview for TMEM132E antibody (C-Term) (ABIN655434)
Target
See all TMEM132E Antibodies
TMEM132E
(Transmembrane Protein 132E (TMEM132E))
Reactivity
Mouse, Human
Host
Rabbit
Clonality
Polyclonal
Conjugate
This TMEM132E antibody is un-conjugated
Application
Western Blotting (WB), Flow Cytometry (FACS)
Clone
RB29313
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Binding Specificity
- 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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Immunogen
- 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 Reactivity: Mouse, Rat WB Host: Rabbit Polyclonal unconjugated
anti-Transmembrane Protein 132E (TMEM132E) antibodyTMEM132E Reactivity: Mouse WB Host: Rabbit Polyclonal unconjugated
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Application Notes
- 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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Preservative
- Sodium azide
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Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
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Storage
- 4 °C,-20 °C
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Storage Comment
- 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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Expiry Date
- 6 months
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: "Whole-exome sequencing identifies a variant in TMEM132E causing autosomal-recessive nonsyndromic hearing loss DFNB99." in: 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." in: Human mutation, Vol. 36, Issue 1, pp. 98-105, (2015) (PubMed).
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