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DYRK1A Polyclonal antibody, PBS Only

DYRK1A Polyclonal Antibody for WB, Indirect ELISA

Cat No. 28607-1-PBS

Host / Isotype

Rabbit / IgG

Reactivity

human

Applications

WB, Indirect ELISA

DYRK, DYRK1, hMNB, HP86, MNB

Formulation:  PBS Only
Conjugate:  Unconjugated
Size/Concentration: 

-/ -

Freight/Packing: -

Quantity

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Product Information

28607-1-PBS targets DYRK1A in WB, Indirect ELISA applications and shows reactivity with human samples.

Tested Reactivity human
Host / Isotype Rabbit / IgG
Class Polyclonal
Type Antibody
Immunogen

CatNo: Ag29433

Product name: Recombinant human DYRK1A protein

Source: e coli.-derived, PGEX-4T

Tag: GST

Domain: 525-763 aa of NM_001396

Sequence: GRARSDPTHQHRHSGGHFTAAVQAMDCETHSPQVRQQFPAPLGWSGTEAPTQVTVETHPVQETTFHVAPQQNALHHHHGNSSHHHHHHHHHHHHHGQQALGNRTRPRVYNSPTNSSSTQDSMEVGHSHHSMTSLSSSTTSSSTSSSSTGNQGNQAYQNRPVAANTLDFGQNGAMDVNLTVYSNPRQETGIAGHPTYQFSANTGPAHYMTEGHLTMRQGADREESPMTGVCVQQSPVASS

Predict reactive species
Full Name dual-specificity tyrosine-(Y)-phosphorylation regulated kinase 1A
Calculated Molecular Weight 86 kDa
Observed Molecular Weight70kDa, 85 kDa
GenBank Accession NumberNM_001396
Gene Symbol DYRK1A
Gene ID (NCBI) 1859
RRIDAB_3086069
Conjugate Unconjugated
FormLiquid
Purification MethodAntigen affinity purification
UNIPROT IDQ13627
Storage Buffer PBS only, pH 7.3.
Storage ConditionsStore at -80°C.

Background Information

This gene encodes a member of the Dual-specificity tyrosine phosphorylation-regulated kinase (DYRK) family. This member contains a nuclear targeting signal sequence, a protein kinase domain, a leucine zipper motif, and a highly conservative 13-consecutive-histidine repeat. It catalyzes its autophosphorylation on serine/threonine and tyrosine residues. It may play a significant role in a signaling pathway regulating cell proliferation and may be involved in brain development. This gene is a homolog of Drosophila mnb (minibrain) gene and rat Dyrk gene. It is localized in the Down syndrome critical region of chromosome 21, and is considered to be a strong candidate gene for learning defects associated with Down syndrome.

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