TUFM antibody (Middle Region)
Quick Overview for TUFM antibody (Middle Region) (ABIN2787734)
Target
See all TUFM (Tufm) AntibodiesReactivity
Host
Clonality
Conjugate
Application
-
-
Binding Specificity
- Middle Region
-
Sequence
- PEKELAMPGE DLKFNLILRQ PMILEKGQRF TLRDGNRTIG TGLVTNTLAM
-
Predicted Reactivity
- Cow: 93%, Dog: 100%, Guinea Pig: 93%, Horse: 93%, Human: 100%, Mouse: 86%, Rabbit: 93%, Rat: 93%, Yeast: 77%, Zebrafish: 86%
-
Characteristics
- This is a rabbit polyclonal antibody against TUFM. It was validated on Western Blot using a cell lysate as a positive control.
-
Purification
- Affinity Purified
-
Immunogen
- The immunogen is a synthetic peptide directed towards the middle region of human TUFM
-
-
-
-
Application Notes
- Optimal working dilutions should be determined experimentally by the investigator.
-
Comment
-
Antigen size: 455 AA
-
Restrictions
- For Research Use only
-
-
-
Format
- Liquid
-
Concentration
- Lot specific
-
Buffer
- Liquid. Purified antibody supplied in 1x PBS buffer with 0.09 % (w/v) sodium azide and 2 % sucrose.
-
Preservative
- Sodium azide
-
Precaution of Use
- This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
-
Handling Advice
- Avoid repeated freeze-thaw cycles.
-
Storage
- -20 °C
-
Storage Comment
- For short term use, store at 2-8°C up to 1 week. For long term storage, store at -20°C in small aliquots to prevent freeze-thaw cycles.
-
-
-
: "hCOA3 stabilizes cytochrome c oxidase 1 (COX1) and promotes cytochrome c oxidase assembly in human mitochondria." in: The Journal of biological chemistry, Vol. 288, Issue 12, pp. 8321-31, (2013) (PubMed).
-
: "hCOA3 stabilizes cytochrome c oxidase 1 (COX1) and promotes cytochrome c oxidase assembly in human mitochondria." in: The Journal of biological chemistry, Vol. 288, Issue 12, pp. 8321-31, (2013) (PubMed).
-
- TUFM (Tufm) (Tu Translation Elongation Factor, Mitochondrial (Tufm))
-
Alternative Name
- TUFM
-
Background
-
TUFM is 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. 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. Publication Note: This RefSeq record includes a subset of the publications that are available for this gene. Please see the Entrez Gene record to access additional publications.
Alias Symbols: COXPD4, EF-TuMT, EFTU, P43
Protein Interaction Partner: FAM9B, FUNDC1, CMTM5, ARL6IP1, HUWE1, FUS, SUMO2, SUMO3, SPRTN, UBC, MDM2, ASB12, ASB14, ASB10, ASB17, SUZ12, BMI1, RNF2, TUBB2A, XPO1, TUBB6, CAMK1D, NSFL1C, IPO9, UBXN1, DCPS, PROSC, PDIA4, PLAA, GTF3C4, NAE1, PPP5C, PPP1R2, PAFAH1B2, HK1, HEXB, GAPDH,
Protein Size: 455 -
Molecular Weight
- 50 kDa
-
Gene ID
- 7284
-
NCBI Accession
- NM_003321, NP_003312
-
UniProt
- P49411
Target
-