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FoxL2 (phospho Ser263) rabbit pAb

CAT: 0855-ES7261-01Size: 50 µLDry Ice: NoHazardous: No
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Background
This gene encodes a forkhead transcription factor. The protein contains a fork-head DNA-binding domain and may play a role in ovarian development and function. Expansion of a polyalanine repeat region and other mutations in this gene are a cause of blepharophimosis syndrome and premature ovarian failure 3. [provided by RefSeq, Jul 2016]
Description
This gene encodes a forkhead transcription factor. The protein contains a fork-head DNA-binding domain and may play a role in ovarian development and function. Expansion of a polyalanine repeat region and other mutations in this gene are a cause of blepharophimosis syndrome and premature ovarian failure 3. [provided by RefSeq, Jul 2016],
Product Name Alternative
FOXL2; Forkhead box protein L2
UniProt
P58012
Swiss Prot
P58012
Reactivity
Human; Mouse
Immunogen
The antiserum was produced against synthesized peptide derived from human FOXL2 around the phosphorylation site of Ser263. AA range:229-278
Target
FoxL2
Clonality
Polyclonal
Source
Rabbit
Applications
WB; ELISA
Concentration
1 mg/ml
Dilution
Western Blot: 1/500 - 1/2000. ELISA: 1/20000. Not yet tested in other applications.
Buffer
-20°C/1 year
Molecular Weight
40kD
Storage Conditions
-20°C/1 year
Observed Molecular Weight
40kD
Fragment
IgG
Subcellular Location
Nucleus .
Other Product Names
FOXL2; Forkhead box protein L2
Gene ID (Human)
668

UniProtKB · P58012

Forkhead box protein L2

FOXL2_HUMAN · Homo sapiens

View on UniProt ↗
Primary accession
P58012
Review status
UniProtKB reviewed (Swiss-Prot)
Gene
FOXL2
Protein existence
1: Evidence at protein level
Organism
Homo sapiens (Human)
Taxonomy ID
9606
Alternative names
—
EC number
—
Processing
—
Secondary accessions
Q4ZGJ3
Protein keywords

Technical term

3D-structureProteomics identificationReference proteome

Biological process

DifferentiationTranscriptionTranscription regulation

Disease

Disease variantPremature ovarian failure

Molecular function

DNA-binding

PTM

Isopeptide bondPhosphoproteinUbl conjugation

Cellular component

Nucleus

Coding sequence diversity

Triplet repeat expansion

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