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Merck

SAB4200034

Sigma-Aldrich

Anti-BMI1 (C-terminal) antibody produced in rabbit

~1.0 mg/mL, affinity isolated antibody, buffered aqueous glycerol solution

Sinónimos:

Anti-B lymphoma Mo-MLV insertion region 1 homolog, Anti-PCGF4, Anti-Polycomb group RING finger protein 4, Anti-RNF51, Anti-Ring finger protein 51

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About This Item

Código UNSPSC:
12352203
NACRES:
NA.41

origen biológico

rabbit

conjugado

unconjugated

forma del anticuerpo

affinity isolated antibody

tipo de anticuerpo

primary antibodies

clon

polyclonal

Formulario

buffered aqueous glycerol solution

mol peso

antigen ~37 kDa

reactividad de especies

human

envase

antibody small pack of 25 μL

concentración

~1.0 mg/mL

técnicas

immunoprecipitation (IP): 2.5-5 μg using lysates of HEK-293T cells over expressing human BMI1
indirect immunofluorescence: 1-2 μg/mL using paraformaldehyde fixed HEK-293T cells over expressing human BMI1
western blot: 2-4 μg/mL using lysates of HEK-293T cells over expressing human BMI1

Nº de acceso UniProt

Condiciones de envío

dry ice

temp. de almacenamiento

−20°C

modificación del objetivo postraduccional

unmodified

Información sobre el gen

human ... BMI1(648)

Descripción general

Anti-BMI1 (C-terminal) is produced in rabbit using as the immunogen a synthetic peptide corresponding to a sequence at the C-terminal of human BMI1, conjugated to KLH. The human proto-oncogene BMI1 (also known as polycomb complex protein BMI-1, polycomb group RING finger protein 4, and RING finger protein 51) is a member of the mammalian Polycomb group (Pc-G) genes.

Aplicación

Anti-BMI1 (C-terminal) antibody produced in rabbit has been used in:
  • western blotting
  • immunoprecipitation
  • immunofluorescence

Acciones bioquímicas o fisiológicas

BMI1 (Proto-Oncogene, Polycomb Ring Finger) plays an important role as epigenetic gene silencers during development. Elevated expression of BMI1 is associated with many cancers such as mantle cell lymphoma, B-cell non-Hodgkin′s lymphoma, myeloid leukemia, non-small cell lung cancer, colorectal cancer, breast cancer and prostate cancer. BMI1 has been shown to be also required for self-renewal of hematopoietic stem cells and neuronal stem cells. BMI1 knockout in mice results in defects in hematopoiesis, skeletal patterning and neurological functions.

Forma física

Solution in 0.01 M phos­phate buffered saline, pH 7.4, containing 15 mM sodium azide.

Cláusula de descargo de responsabilidad

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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Código de clase de almacenamiento

10 - Combustible liquids

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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Bmi-1 cooperates with H-Ras to transform human mammary epithelial cells via dysregulation of multiple growth-regulatory pathways
Datta S, et al.
Cancer Research, 67(21), 10286-10295 (2007)
Bmi-1 is required for maintenance of adult self-renewing haematopoietic stem cells
Park I K, et al.
Nature, 423(6937), 302-302 (2003)
Bmi1, stem cells, and senescence regulation
Park IK, et al.
The Journal of Clinical Investigation, 113(2), 175-179 (2004)
Bmi-1 dependence distinguishes neural stem cell self-renewal from progenitor proliferation
Molofsky AV, et al.
Nature, 425(6961), 962-962 (2003)
Zhaocheng Zhang et al.
Cancer research, 74(10), 2869-2881 (2014-04-02)
Emerging evidence suggests that endothelial cell-secreted factors contribute to the pathobiology of squamous cell carcinoma (SCC) by enhancing invasive migration and resistance to anoikis. Here, we report that SCC cells within the perivascular niche have undergone epithelial to mesenchymal transition

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