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  • Featured Product
  • KD/KO Validated

AlaRS Monoclonal antibody, PBS Only

AlaRS Monoclonal Antibody for WB, IF/ICC, Indirect ELISA

Host / Isotype

Mouse / IgG1

Reactivity

Human, Mouse, Rat

Applications

WB, IF/ICC, Indirect ELISA

Conjugate

Unconjugated

CloneNo.

1C8H3

Cat no : 67909-1-PBS

Synonyms

AARS, Alanine tRNA ligase, alanyl tRNA synthetase, AlaRS

Validation Data Gallery

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  • Western Blot (WB) analysis of various lysates using AlaRS Monoclonal antibody (67909-1-Ig)

    WB analysis using 67909-1-Ig (same clone as 67909-1-PBS)

    Various lysates were subjected to SDS PAGE followed by western blot with 67909-1-Ig (AlaRS antibody) at dilution of 1:10000 incubated at room temperature for 1.5 hours. The membrane was stripped and reblotted with Lamin B1 Monoclonal antibody (66095-1-Ig) as loading control. This data was developed using the same antibody clone with 67909-1-PBS in a different storage buffer formulation.

  • Western Blot (WB) analysis of HeLa cells using AlaRS Monoclonal antibody (67909-1-Ig)

    WB analysis of HeLa using 67909-1-Ig (same clone as 67909-1-PBS)

    WB result of AlaRS antibody (67909-1-Ig; 1:6000; incubated at room temperature for 1.5 hours) with sh-Control and sh-AlaRS transfected HeLa cells. This data was developed using the same antibody clone with 67909-1-PBS in a different storage buffer formulation.

  • Western Blot (WB) analysis of various lysates using AlaRS Monoclonal antibody (67909-1-Ig)

    WB analysis using 67909-1-Ig (same clone as 67909-1-PBS)

    Various lysates were subjected to SDS PAGE followed by western blot with 67909-1-Ig (AARS antibody) at dilution of 1:10000 incubated at room temperature for 1.5 hours. This data was developed using the same antibody clone with 67909-1-PBS in a different storage buffer formulation.

  • Immunofluorescence (IF) / fluorescent staining of HepG2 cells using AlaRS Monoclonal antibody (67909-1-Ig)

    IF Staining of HepG2 using 67909-1-Ig (same clone as 67909-1-PBS)

    Immunofluorescent analysis of (-20°C Ethanol) fixed HepG2 cells using AlaRS antibody (67909-1-Ig, Clone: 1C8H3 ) at dilution of 1:400 and CoraLite®488-Conjugated Goat Anti-Mouse IgG(H+L) (SA00013-1). This data was developed using the same antibody clone with 67909-1-PBS in a different storage buffer formulation.

  • Immunofluorescence (IF) / fluorescent staining of A431 cells using AlaRS Monoclonal antibody (67909-1-Ig)

    IF Staining of A431 using 67909-1-Ig (same clone as 67909-1-PBS)

    Immunofluorescent analysis of (-20°C Methanol) fixed A431 cells using AlaRS antibody (67909-1-Ig, Clone: 1C8H3 ) at dilution of 1:400 and CoraLite®488-Conjugated Goat Anti-Mouse IgG(H+L). This data was developed using the same antibody clone with 67909-1-PBS in a different storage buffer formulation.

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Tested Applications

Recommended dilution

ApplicationDilution
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.

Product Information

67909-1-PBS targets AlaRS in WB, IF/ICC, Indirect ELISA applications and shows reactivity with Human, Mouse, Rat samples.

Tested Reactivity Human, Mouse, Rat
Host / Isotype Mouse / IgG1
Class Monoclonal
Type Antibody
Immunogen AlaRS fusion protein Ag11151 相同性解析による交差性が予測される生物種
Full Name alanyl-tRNA synthetase
Calculated molecular weight 968 aa, 107 kDa
Observed molecular weight107 kDa
GenBank accession numberBC011451
Gene symbol AlaRS
Gene ID (NCBI) 16
Conjugate Unconjugated
Form Liquid
Purification MethodProtein A purification
Storage Buffer PBS Only
Storage ConditionsStore at -80°C.

Background Information

AARS(alanyl-tRNA synthetase) is also named as AlaRS(alanine tRNA ligase 1, cytoplasmic), renal carcinoma antigen NY-REN-42 and belongs to the class-II aminoacyl-tRNA synthetase family. It can interpret the RNA code and attach specific aminoacids to the tRNAs that contain the cognate trinucleotide anticodons. AARS consists of three domains: the N-terminal catalytic domain, the editing domain and the C-terminal C-Ala domain. The editing domain removes incorrectly charged amino acids, while the C-Ala domain, along with tRNA(Ala), serves as a bridge to cooperatively bring together the editing and aminoacylation centers thus stimulating deacylation of misacylated tRNAs(PMID:19661429).