KD-Validated LATS1 Mouse Oligoclonal Antibody
Size:20μL Price:$118
Size:50μL Price:$218
Size:100μL Price:$318
Application:WB

Reactivity:Human,Rat
Conjugate:Unconjugated
Gene Name:LATS1
SKU: KVAb01094
Detail

Summary

Production Name

KD-Validated LATS1 Mouse Oligoclonal Antibody

Description

KD-Validated antibody

Host

Mouse

Application

WB

Reactivity

Human,Rat

 

Performance

Conjugation

Unconjugated

Modification

Unmodified

Isotype

Mouse IgG

Clonality

Mouse oligoclonal antibody

Form

Liquid

Storage

Store at 4°C short term. Aliquot and store at -20°C long term. Avoid freeze/thaw cycles.

Buffer

Supplied in PBS (pH 7.4) containing 50% glycerol, and 0.02% sodium azide.

Purification

Affinity purification

 

Immunogen

Gene Name

LATS1

Alternative Names

LATS1; Large Tumor Suppressor Kinase 1; WARTS; LATS (Large Tumor Suppressor, Drosophila) Homolog 1; Serine/Threonine-Protein Kinase LATS1; Large Tumor Suppressor Homolog 1; WARTS Protein Kinase; EC 2.7.11.1; H-Warts; LATS, Large Tumor Suppressor, Homolog 1 (Drosophila); LATS, Large Tumor Suppressor, Homolog 1; EC 2.7.11; Wts

Gene ID

9113

SwissProt ID

O95835

 

Application

Dilution Ratio

WB 1:500-1:2,500

Molecular Weight

Calculated MW: 126.9kDa

 

Background

The protein encoded by this gene is a putative serine/threonine kinase that localizes to the mitotic apparatus and complexes with cell cycle controller CDC2 kinase in early mitosis. The protein is phosphorylated in a cell-cycle dependent manner, with late prophase phosphorylation remaining through metaphase. The N-terminal region of the protein binds CDC2 to form a complex showing reduced H1 histone kinase activity, indicating a role as a negative regulator of CDC2/cyclin A. In addition, the C-terminal kinase domain binds to its own N-terminal region, suggesting potential negative regulation through interference with complex formation via intramolecular binding. Biochemical and genetic data suggest a role as a tumor suppressor. This is supported by studies in knockout mice showing development of soft-tissue sarcomas, ovarian stromal cell tumors and a high sensitivity to carcinogenic treatments. [provided by RefSeq, Apr 2017]

 

Research Area

Cell Biology,Cancer

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