ARMC4 Recombinant monoclonal antibody

ARMC4 Uni-rAb® Recombinant Antibody for WB, ELISA
Cat No. 84004-3-RR
Clone No.241122G4

Host / Isotype

Rabbit / IgG

Reactivity

human, mouse

Applications

WB, ELISA

RP11 691I13.1, Outer dynein arm-docking complex subunit 2, ODAD2, Armadillo repeat-containing protein 4, armadillo repeat containing 4

Formulation:  PBS and Azide
PBS and Azide
PBS Only
Conjugate:  Unconjugated
Unconjugated
Size/Concentration: 

-/ -


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保証・サポートについて

テクニカルサポートまたはご購入後1年間の交換/補填対応を承ります。詳細はこちらをご覧ください。


Tested Applications

Positive WB detected inmouse testis tissue

Recommended dilution

ApplicationDilution
Western Blot (WB)WB : 1:1000-1:4000
It is recommended that this reagent should be titrated in each testing system to obtain optimal results.
Sample-dependent, Check data in validation data gallery.

Product Information

84004-3-RR targets ARMC4 in WB, ELISA applications and shows reactivity with human, mouse samples.

Tested Reactivity human, mouse
Host / Isotype Rabbit / IgG
Class Recombinant
Type Antibody
Immunogen ARMC4 fusion protein Ag22340 相同性解析による交差性が予測される生物種
Full Name armadillo repeat containing 4
Calculated molecular weight 1044 aa, 116 kDa
Observed molecular weight116 kDa
GenBank accession numberBC140846
Gene Symbol ODAD2
Gene ID (NCBI) 55130
RRIDAB_3671575
Conjugate Unconjugated
Form
FormLiquid
Purification MethodProtein A purfication
UNIPROT IDQ5T2S8
Storage Buffer PBS with 0.02% sodium azide and 50% glycerol{{ptg:BufferTemp}}7.3
Storage ConditionsStore at -20°C. Stable for one year after shipment. Aliquoting is unnecessary for -20oC storage.

Background Information

ODAD2 contains ten Armadillo repeat motifs (ARMs) and one HEAT repeat, and is thought to be involved in ciliary and flagellar movement. This protein has been shown to localize to the ciliary axonemes and at the ciliary base of respiratory cells. Studies indicate that mutations in this gene cause partial outer dynein arm (ODA) defects in respiratory cilia. The cilia of cells with mutations in this gene displayed either reduced ciliary beat frequency and amplitude, or, complete immotility. Some individuals with primary ciliary dyskensia (PCD) have been shown to have mutations in this gene. PCD is characterized by chronic airway disease and left/right body asymmetry defects.

Protocols

Product Specific Protocols
WB protocol for ARMC4 antibody 84004-3-RRDownload protocol
Standard Protocols
Click here to view our Standard Protocols
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