No products in the cart.
Rabbit Anti-LARS2 Antibody (CSB-PA613580ESR1HU)
Supplier: CUSABIO BIOTECH CO.
Probable leucine–tRNA ligase Antibody,mitochondrial Antibody,Leucyl-tRNA synthetase Antibody,LeuRS Antibody,LARS2 Antibody,KIAA0028 AntibodyMore alternative names for the antibody
KIAA0028 antibody|LARS 2 antibody|Lars2 antibody|Leucine translase antibody|Leucine tRNA ligase 2 antibody|Leucine tRNA ligase 2 mitocondrial antibody|Leucine tRNA ligase antibody|Leucine–tRNA ligase antibody|Leucyl tRNA synthetase 2 antibody|Leucyl tRNA synthetase 2 mitochondrial antibody|LeuRS antibody|MGC26121 antibody|Probable leucyl-tRNA synthetase, mitochondrial antibody|SYLM_HUMAN antibody
Anti-LARS2 antibody (ab96221)
Anti-LARS2 antibody (ab96221)
Recommended applications: ELISA, IHC
Recommended dilution: Recommended dilution:IHC:1:20-1:200
Recommended protocols: check protocols
|Catalogue No.|| |
Recombinant human Probable leucine–tRNA ligase, mitochondrial protein (1-250AA)
|Recommended dilution|| |
|Molecular weight|| |
Antigen Affinity Purified
Shipped at 4 Celcius Degree. Upon delivery aliquot and store at -20 Celcius Degree or -80 Celcius Degree. Avoid repeated freeze.
|Database links|| |
Entrez Gene:504609( Cow), Entrez Gene:23395( Human), Entrez Gene:102436( Mouse), Omim:604544( Human), SwissProt:Q15031( Human), SwissProt:Q8VDC0( Mouse), Unigene:526975( Human), Unigene:276076( Mouse)
|Protein tissue specificity|| |
Ubiquitously expressed, but highest expression in tissues with high metabolic rates, such as skeletal muscle, heart, and kidney. .
|Involvement in disease|| |
Perrault syndrome 4 (PRLTS4) [MIM:615300]: A sex-influenced disorder characterized by sensorineural deafness in both males and females, and ovarian dysgenesis in females. Affected females have primary amenorrhea, streak gonads, and infertility, whereas affected males show normal pubertal development and are fertile. . Note=The disease is caused by mutations affecting the gene represented in this entry.; Hydrops, lactic acidosis, and sideroblastic anemia (HLASA) [MIM:617021]: A lethal, multisystem metabolic disorder characterized by severe lactic acidosis, hydrops, and sideroblastic anemia. Additional features include impaired cardiac function, disordered coagulation, pulmonary hypertension, and progressive renal disease. . Note=The disease is caused by mutations affecting the gene represented in this entry.
|Protein sequence and domain|| |
Belongs to the class-I aminoacyl-tRNA synthetase family.
|Protein cellular localization|| |
Mitochondrion matrix .
AntibodyPlus provides antibody trial sample for your own antibody validation and collects antibody reviews.
CUSABIO BIOTECH CO.
|Product type|| |
There are no reviews for this product yet.
By submitting a review, get following benefits:
1. Receive $50 ABcoins as credit for each review.
2. First trial sample order will be fully refunded as credit.
3. Have a chance to win a $50 amazon gift card!
There is no extra validation for this product yet.
Check other extra validated antibodies below: