BioMall
Brand Store/EnkiLife/Phospho-FoxL2 (Ser263) Rabbit Polyclonal Antibody
Phospho-FoxL2 (Ser263) Rabbit Polyclonal Antibody
BRAND STORE

Phospho-FoxL2 (Ser263) Rabbit Polyclonal Antibody

APRab04691-20μL · 20μL

EN

Verified Partner

Sign in to see pricing and request a quote.

Brand Store Product

No external links. Get your quote directly here.

Catalog No: APRab04691-20μL
Pack Size: 20μL
Brand: EnkiLife

Description

EnkiLife offers the Phospho-FoxL2 (Ser263) Rabbit Polyclonal Antibody. This antibody reacts with Human,Mouse species and is suitable for WB,ELISA application. Alternative Names of Immunogen: FOXL2; Forkhead box protein L2. The product boasts remarkable high specificity, outstanding reproducibility, and exceptional affinity, making it a reliable and superior choice for your needs. Dilution Ratio: WB 1:500-1:2000,ELISA 1:10000-1:20000 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],disease:Defects in FOXL2 are a cause of blepharophimosis, ptosis, and epicanthus inversus syndrome (BPES) [MIM:110100]; also known as blepharophimosis syndrome. It is an autosomal dominant disorder characterized by eyelid dysplasia, small palpebral fissures, drooping eyelids and a skin fold running inward and upward from the lower lid. In type I BPSE (BPES1) eyelid abnormalities are associated with female infertility. Affected females show an ovarian deficit due to primary amenorrhea or to premature ovarian failure (POF). In type II BPSE (BPES2) affected individuals show only the eyelid defects. There is a mutational hotspot in the region coding for the poly-Ala domain, since 30% of all mutations in the ORF lead to poly-Ala expansions, resulting mainly in BPES type II.,disease:Defects in FOXL2 are a cause of premature ovarian failure 3 (POF3) [MIM:608996]. Premature ovarian failure (POF) is a defect of ovarian development and is characterized by hypoestrogenism, primary or secondary amenorrhea, with elevated levels of serum gonadotropins, or by early menopause. POF is defined as the cessation of ovarian function under the age of 40 years.,function:Probable transcriptional regulator.,similarity:Contains 1 fork-head DNA-binding domain.,tissue specificity:In addition to its expression in the developing eyelid, it is transcribed very early in somatic cells of the developing gonad (before sex determination) and its expression persists in the follicular cells of the adult ovary.,

More from EnkiLife

Bok Rabbit Monoclonal Antibody
Bok Rabbit Monoclonal Antibody
AMRe86804-20μL
NR3C1 Mouse Monoclonal Antibody
NR3C1 Mouse Monoclonal Antibody
AMM80942-50μL
SUN2 Rabbit Monoclonal Antibody
SUN2 Rabbit Monoclonal Antibody
AMRe86176-20μL
KD-Validated GAPDH Recombinant Rabbit Monoclonal Antibody
KD-Validated GAPDH Recombinant Rabbit Monoclonal Antibody
KVAb00025-100ul
Human GRb (Glucocorticoid Receptor Beta) ELISA Kit
Human GRb (Glucocorticoid Receptor Beta) ELISA Kit
EH24837-96T
ERBB3 Mouse Monoclonal Antibody
ERBB3 Mouse Monoclonal Antibody
AMM80758-50μL
BDH1 Mouse Monoclonal Antibody
BDH1 Mouse Monoclonal Antibody
AMM80811-100μL
NOC2L Rabbit Polyclonal Antibody
NOC2L Rabbit Polyclonal Antibody
APRab14774-50μL