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Merck

SAB4200270

Sigma-Aldrich

Anti-PSMB9 antibody, Mouse monoclonal

clone LMP2-37, purified from hybridoma cell culture

Sinónimos:

Monoclonal Anti-LMP2, Monoclonal Anti-PSMB6i, Monoclonal Anti-RING12, Monoclonal Anti-beta1i, Monoclonal Anti-proteasome (prosome, macropain) subunit, beta type, 9 (large multifunctional peptidase 2)

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About This Item

Código UNSPSC:
12352203

origen biológico

mouse

conjugado

unconjugated

forma del anticuerpo

purified from hybridoma cell culture

tipo de anticuerpo

primary antibodies

clon

LMP2-37, monoclonal

formulario

buffered aqueous solution

mol peso

antigen 17 kDa

reactividad de especies

human, mouse, rat

concentración

~1.0 mg/mL

técnicas

immunocytochemistry: suitable
indirect ELISA: suitable
western blot: 1.0-2.0 μg/mL using extracts of rat spleen

isotipo

IgG2a

Nº de acceso UniProt

Condiciones de envío

dry ice

temp. de almacenamiento

−20°C

modificación del objetivo postraduccional

unmodified

Información sobre el gen

human ... PSMB9(5698)

Descripción general

Monoclonal Anti-PSMB9 (mouse IgG2a isotype) is derived from the hybridoma LMP2-37 produced by the fusion of mouse myeloma cells and splenocytes from BALB/c mice immunized with human PSMB9 recombinant protein. Proteasome 20S subunit beta 9 (PSMB9) is present in the major histocompatibility complex (MHC) class II region. γ-interferon triggers the synthesis of three proteasomal subunits-PSMB9 (β1i), PSMB10 (β2i) and PSMB8 (β5i), which is a part of immunoproteasome.

Inmunógeno

human PSMB9, recombinant protein.

Aplicación

Monoclonal Anti-PSMB9 antibody produced in mouse has been used in:
  • flow cytometry
  • enzyme linked immunosorbent assay (ELISA)
  • immunoblotting
  • immunocytochemistry

Acciones bioquímicas o fisiológicas

Proteasome 20S subunit beta 9 (PSMB9) is used during antigen presentation. Aberrant levels of PSMB9 is involved in autoimmune disorders such as primary Sjogren′s syndrome and uterine leiomyosarcomas. The proteasome is a multicatalytic proteinase complex, which is involved in the regulation of essential cellular processes such as transcription, cell cycle progression, differentiation, apoptosis and in the control of stress and immune responses.

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

12 - Non Combustible Liquids

Clase de riesgo para el agua (WGK)

WGK 1

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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Visite la Librería de documentos

Aaron Javitt et al.
Frontiers in immunology, 10, 141-141 (2019-03-06)
Antigen presentation on HLA molecules is a major mechanism by which the immune system monitors self and non-self-recognition. Importantly, HLA-I presentation has gained much attention through its role in eliciting anti-tumor immunity. Several determinants controlling the peptides presented on HLA
Proteasome and peptidase function in MHC-class-I-mediated antigen presentation
Kloetzel PM and Ossendorp F
Current Opinion in Immunology, 16(1), 76-81 (2004)
The ubiquitin-proteasome system and its role in inflammatory and autoimmune diseases
Wang J, et al.
Cellular & Molecular Immunology, 3(4), 255-261 (2006)
Pro-inflammatory cytokines alter the immunopeptidome landscape by modulation of HLA-B expression
Javitt A, et al.
Frontiers in immunology, 10, 141-141 (2019)
Tight junction protein 1 modulates proteasome capacity and proteasome inhibitor sensitivity in multiple myeloma via EGFR/JAK1/STAT3 signaling
Zhang XD, et al.
Cancer Cell, 29(5), 639-652 (2016)

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