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Merck

M4278

Sigma-Aldrich

Monoclonal Anti-MAP1 antibody produced in mouse

clone HM-1, ascites fluid

Sinónimos:

Anti-MAP1a

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About This Item

Número MDL:
Código UNSPSC:
12352203
NACRES:
NA.41

origen biológico

mouse

conjugado

unconjugated

forma del anticuerpo

ascites fluid

tipo de anticuerpo

primary antibodies

clon

HM-1, monoclonal

contiene

15 mM sodium azide

reactividad de especies

mouse, rat

técnicas

immunohistochemistry (frozen sections): suitable
microarray: suitable
western blot: 1:500 using a fresh total rat brain extract or an enriched microtubule protein preparation

isotipo

IgG1

Nº de acceso UniProt

Condiciones de envío

dry ice

temp. de almacenamiento

−20°C

modificación del objetivo postraduccional

unmodified

Información sobre el gen

mouse ... Mtap1a(17754)
rat ... Map1a(25152)

Categorías relacionadas

Descripción general

Monoclonal Anti-MAP1 (mouse IgG1 isotype) is derived from the HM-1 hybridoma produced by the fusion of mouse myeloma cells and splenocytes from BALB/c mice immunized with a rat brain MAPs preparation. MAP1 is one of the major neuronal MAPs as well as being the largest (350 kD). MAP1 is more generally distributed, being found in both dendrites and axons of neurons and in glial cells in brain, in chromatophores and on both interphase and mitotic microtubules in various tissue culture cells.

Especificidad

The antibody does not cross-react with other MAPs or tubulin. By immunohistochemical staining of brain tissue, the antibody shows selective labeling of neurons with stronger staining of axons than dendrites.

Inmunógeno

rat brain microtubule-associated proteins (MAPs)

Aplicación

Monoclonal Anti-MAP1 has been used in :
  • immunoblotting
  • dot blot
  • immunocytochemistry
  • immunohistochemistry

Acciones bioquímicas o fisiológicas

Microtubules are the ubiquitous cytoskeletal structural components that are involved in intracellular transport. They are composed of tubulin and microtubule-associated proteins (MAPs). MAPs are known to mediate the binding of membranous organelles, actin filaments and intermediate filaments to microtubules. Therefore, it might be important for cellular processes such as mitosis and organelle transport, and for determining the dynamic properties of the cytoskeleton.

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

Clase de riesgo para el agua (WGK)

WGK 1


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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Cytoskeletons in the Closet-Subversion in Alphaherpesvirus Infections
Denes C, et al.
Viruses, 10(2), 79-79 (2018)
Drosophila Futsch/22C10 is a MAP1B-like protein required for dendritic and axonal development
Hummel T, et al.
Neuron, 26(2), 357-370 (2000)
The calcium-sensitive large-conductance potassium channel (BK/MAXI K) is present in the inner mitochondrial membrane of rat brain
Douglas RM, et al.
Neuroscience, 139(4), 1249-1261 (2006)
Alan Jerusalmi et al.
Molecular therapy : the journal of the American Society of Gene Therapy, 8(6), 886-894 (2003-12-11)
We have initiated studies to determine the feasibility of employing the Semliki Forest virus (SFV) expression system as a central nervous system (CNS) vector. We investigated the effects of infecting Balb/c mice intranasally (i.n.) with recombinant SFV particles expressing the
Effect of intranasal administration of semliki forest virus recombinant particles expressing reporter and cytokine genes on the progression of experimental autoimmune encephalomyelitis
Jerusalmi A, et al.
Molecular Therapy, 8(6), 886-894 (2003)

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