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F0805

Anti-FOXL2 antibody produced in rabbit

affinity isolated antibody

Sinonimo/i:

Anti-Forkhead L2, Anti-Forkhead Transcription Factor

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Taglio della confezioneSKUDisponibilitàPrezzo
100 μg
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CHF 461.00

Informazioni su questo articolo

UNSPSC Code:
12352203
NACRES:
NA.41
MDL number:
Conjugate:
unconjugated
Clone:
polyclonal
Application:
IF, IHC (p), WB
Citations:
8

CHF 461.00


Per conoscere la disponibilità, visualizza il carrello

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biological source

rabbit

Quality Level

conjugate

unconjugated

antibody form

affinity isolated antibody

antibody product type

primary antibodies

clone

polyclonal

species reactivity

mouse, hamster

technique(s)

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 accession no.

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Gene Information

mouse ... Foxl2(26927)

General description

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.

Immunogen

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.

Application

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.

Biochem/physiol Actions

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.

Physical form

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.

Disclaimer

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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WH0002300M3WH0002303M2SAB2500424
conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

conjugate

unconjugated

biological source

rabbit

biological source

mouse

biological source

mouse

biological source

goat

Quality Level

200

Quality Level

-

Quality Level

100

Quality Level

-

antibody form

affinity isolated antibody

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

antibody form

affinity isolated antibody

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

storage temp.

−20°C

clone

polyclonal

clone

1A7, monoclonal

clone

2H3, monoclonal

clone

polyclonal


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Classe di stoccaggio

10 - Combustible liquids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, multi-purpose combination respirator cartridge (US)



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Contenuto correlato

Instructions


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
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
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



Numero articolo commerciale globale

SKUGTIN
F0805-100UG04061837771460

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