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Mouse Anti-DARS Recombinant Antibody (CBYCD-153) (CBMAB-D0242-YC)

Provided herein is a Mouse monoclonal antibody, which binds to Aspartyl-TRNA Synthetase (DARS). The antibody can be used for immunoassay techniques, such as ELISA, IHC-P, RNAi, WB.
See all DARS antibodies

Summary

Host Animal
Mouse
Specificity
Human
Clone
CBYCD-153
Antibody Isotype
IgG2a, κ
Application
ELISA, IHC-P, RNAi, WB

Basic Information

Immunogen
DARS (NP_001340, 393 a.a. ~ 501 a.a) partial recombinant protein with GST tag.
Specificity
Human
Antibody Isotype
IgG2a, κ
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.

Formulations & Storage [For reference only, actual COA shall prevail!]

Storage
Store at 4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
aspartyl-tRNA synthetase
Introduction
DARS belongs to a multienzyme complex that functions in mediating the attachment of amino acids to their cognate tRNAs. The encoded protein ligates L-aspartate to tRNA(Asp). Mutations in this gene have been found in patients showing hypomyelination with brainstem and spinal cord involvement and leg spasticity.
Entrez Gene ID
UniProt ID
Alternative Names
Aspartyl-TRNA Synthetase; Cell Proliferation-Inducing Gene 40 Protein; Aspartate TRNA Ligase 1, Cytoplasmic; EC 6.1.1.12; AspRS; Aspartyl-TRNA Synthetase, Cytoplasmic; Aspartate--TRNA Ligase, Cytoplasmic; Testicular Tissue Protein Li 192; HBSL;
Function
Catalyzes the specific attachment of an amino acid to its cognate tRNA in a 2 step reaction: the amino acid (AA) is first activated by ATP to form AA-AMP and then transferred to the acceptor end of the tRNA.
Biological Process
Aspartyl-tRNA aminoacylation Source: GO_Central
Protein-containing complex assembly Source: ProtInc
Translation Source: ProtInc
tRNA aminoacylation for protein translation Source: Reactome
Cellular Location
Cytosol
Involvement in disease
Hypomyelination with brainstem and spinal cord involvement and leg spasticity (HBSL):
An autosomal recessive leukoencephalopathy characterized by onset in the first year of life of severe spasticity, mainly affecting the lower limbs and resulting in an inability to achieve independent ambulation. Affected individuals show delayed motor development and nystagmus; some may have mild mental retardation. Brain MRI shows hypomyelination and white matter lesions in the cerebrum, brainstem, cerebellum, and spinal cord.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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