추천 제품
생물학적 소스
rabbit
Quality Level
결합
unconjugated
항체 형태
affinity isolated antibody
항체 생산 유형
primary antibodies
클론
polyclonal
종 반응성
mouse, hamster
기술
immunohistochemistry (formalin-fixed, paraffin-embedded sections): 0.2 μg/mL using murine prenatal folicle
indirect immunofluorescence: 2 μg/mL using KK1 granulosa cells
western blot: 0.2 μg/mL using CHO whole cell lysate
UniProt 수납 번호
배송 상태
dry ice
저장 온도
−20°C
타겟 번역 후 변형
unmodified
유전자 정보
mouse ... Foxl2(26927)
면역원
synthetic peptide M(1)MASYPEPEDTAGT(14) corresponding to amino acid residues 1-14 from mouse FOXL2. This sequence is completely conserved in mouse and rat and 92% conserved in human.
애플리케이션
Anti-FOXL2 antibody produced in rabbit is suitable for the following applications:
- Immunohistochemistry (formalin-fixed, paraffin-embedded sections) at a concentration of 0.2μg/mL using murine prenatal folicle
- Indirect immunofluorescence at a concentration of 2μg/mL using KK1 granulosa cells
- Western blotting (at a concentration of 0.2μg/mL using CHO whole cell lysate) or immunoblot analysis.
생화학적/생리학적 작용
Forkhead box protein L2 is a protein encoded by the FOXL2 gene in humans. The gene FOXL2 encodes a member of the fork-head-winged-helix family of transcription factors. It is expressed early during female gonadal development and is expressed in normal ovarian stroma and ovarian neoplasms with granulosa cell lineage. FOXL gene encodes an essential transcription factor in the ovary and helps in female sex determination, follicle recruitment and granulosa cell development. Its mutation is specific to AGCTs in the ovary and is useful for diagnosis of disease. FOXL2 acts as an oncogene or tumour suppressor depending on the genetic context that is the GCT subtype.
표적 설명
FOXL2 encodes a forkhead transcription factor. The protein contains a fork-head DNA-binding domain and may play a role in ovarian development and function. Mutations in this gene are a cause of blepharophimosis syndrome and premature ovarian failure 3.
물리적 형태
Provided as 100 μg of affinity purified IgG (1 mg/mL) in phosphate buffered saline containing 1 mg/mL bovine serum albumin and 0.05% sodium azide.
면책조항
Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals.
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Storage Class Code
10 - Combustible liquids
WGK
WGK 3
Flash Point (°F)
Not applicable
Flash Point (°C)
Not applicable
개인 보호 장비
Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)
시험 성적서(COA)
제품의 로트/배치 번호를 입력하여 시험 성적서(COA)을 검색하십시오. 로트 및 배치 번호는 제품 라벨에 있는 ‘로트’ 또는 ‘배치’라는 용어 뒤에서 찾을 수 있습니다.
Fubiao Shi et al.
Human molecular genetics, 23(14), 3792-3800 (2014-02-26)
Blepharophimosis, ptosis, epicanthus inversus syndrome (BPES) is an autosomal dominant genetic disorder characterized by small palpebral fissures and other craniofacial malformations, often with (type I) but could also without (type II) premature ovarian failure. While mutations of the forkhead transcription
Maria Westerhoff et al.
Human pathology, 45(5), 1010-1014 (2014-04-22)
FOXL2, a gene encoding a member of the fork-head-winged-helix family of transcription factors, is one of the earliest expressed genes during female gonadal development. It is expressed in normal ovarian stroma and ovarian neoplasms with granulosa cell lineage. Nonovarian tumors
Roseanne Rosario et al.
Gynecologic oncology, 133(2), 382-387 (2013-12-18)
It has been four years since the discovery of the FOXL2 402C>G mutation in adult ovarian granulosa cell tumours. Yet to date, there have been few studies which have investigated the precise role of the mutation in tumour pathogenesis. This
Akimasa Takahashi et al.
The Tohoku journal of experimental medicine, 231(4), 243-250 (2013-11-22)
Adult-type granulosa cell tumor (AGCT) is a rare class of malignant ovarian tumor with unique features, characterized by slow growth, late recurrence, relatively good prognosis and unified cause in almost all patients. The forkhead box L2 (FOXL2) gene encodes an
Stella Tran et al.
Molecular endocrinology (Baltimore, Md.), 27(3), 407-421 (2013-01-24)
Impairments in pituitary FSH synthesis or action cause infertility. However, causes of FSH dysregulation are poorly described, in part because of our incomplete understanding of mechanisms controlling FSH synthesis. Previously, we discovered a critical role for forkhead protein L2 (FOXL2)
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