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TUFM antibody (C-Term)
Tufm
Reactivity: Human
WB
Host: Rabbit
Polyclonal
RB22085
unconjugated
Product Details anti-TUFM Antibody
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Target
See all TUFM (Tufm) Antibodies
TUFM (Tufm)
(Tu Translation Elongation Factor, Mitochondrial (Tufm))
Binding Specificity
All epitopes for TUFM antibodies
AA 342-370, C-Term
Reactivity
All reactivities for TUFM antibodies
Human
Host
All hosts for TUFM antibodies
Rabbit
Clonality
All clonalities for TUFM antibodies
Polyclonal
Conjugate
All conjugates for TUFM antibodies
This TUFM antibody is un-conjugated
Application
All applications for TUFM antibodies
Western Blotting (WB)
Predicted Reactivity
M, Rat
Purification
This antibody is purified through a protein A column, followed by peptide affinity purification.
Immunogen
This TUFM antibody is generated from rabbits immunized with a KLH conjugated synthetic peptide between 342-370 amino acids from the C-terminal region of human TUFM.
Clone
RB22085
Isotype
Ig Fraction
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Discover our top product Tufm Primary Antibody
Alternatives
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Application Details
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Application Notes
WB: 1:1000
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
Purified polyclonal antibody supplied in PBS with 0.09 % (W/V) sodium azide.
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
4 °C,-20 °C
Storage Comment
TUFM Antibody (C-term) can be refrigerated at 2-8 °C for up to 6 months. For long term storage, place the at -20 °C.
Expiry Date
6 months
Target Details for TUFM
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Target
TUFM (Tufm)
(Tu Translation Elongation Factor, Mitochondrial (Tufm))
Alternative Name
TUFM (Tufm Products )
Synonyms
TUFM antibody, D250 antibody, fi06f04 antibody, wu:fi06f04 antibody, zgc:110766 antibody, COXPD4 antibody, EF-TuMT antibody, EFTU antibody, P43 antibody, 2300002G02Rik antibody, C76308 antibody, C76389 antibody, Tu translation elongation factor, mitochondrial antibody, TUFM antibody, tufm antibody, Tufm antibody
Background
This gene encodes a protein which participates in protein translation in mitochondria. Mutations in this gene have been associated with combined oxidative phosphorylation deficiency resulting in lactic acidosis and fatal encephalopathy. A pseudogene has been identified on chromosome 17.
Molecular Weight
49542
Gene ID
7284
NCBI Accession
NP_003312
UniProt
P49411
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