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Merck

AB1989

Sigma-Aldrich

Anti-Neurofilament H (200 kDa) Antibody

CHEMICON®, rabbit polyclonal

Szinonimák:

Anti-CMT2CC, Anti-NFH

Bejelentkezésa Szervezeti és Szerződéses árazás megtekintéséhez


About This Item

UNSPSC kód:
12352203
eCl@ss:
32160702
NACRES:
NA.41

Terméknév

Anti-Neurofilament H (200 kDa) Antibody, CT, serum, Chemicon®

biológiai forrás

rabbit

Minőségi szint

antitest forma

serum

antitest terméktípus

primary antibodies

klón

polyclonal

faj reaktivitás

bovine, rat, human, pig, mouse

gyártó/kereskedő neve

Chemicon®

technika/technikák

immunohistochemistry: suitable
western blot: suitable

NCBI elérési szám

UniProt elérési szám

kiszállítva

dry ice

célzott transzláció utáni módosítás

unmodified

Géninformáció

bovine ... Nefh(528842)
human ... NEFH(4744)
mouse ... Nefh(380684)
pig ... Nefh(100156492)
rat ... Nefh(24587)

Általános leírás

Neurofilaments are a type of intermediate filament that serve as major elements of the cytoskeleton supporting the axon cytoplasm. They are the most abundant fibrillar components of the axon, being on average 3-10 times more frequent than axonal microtubules. Neurofilaments (10nm in dia.) are built from three intertwined protofibrils which are themselves composed of two tetrameric protofilament complexs of monomeric proteins. The neurofilament triplet proteins (68/70, 160, and 200 kDa) occur in both the central and peripheral nervous system and are usually neuron specific. The 68/70 kDa NF-L protein can self-assemble into a filamentous structure, however the 160 kDa NF-M and 200 kDa NF-H proteins require the presence of the 68/70 kDa NF-L protein to co-assemble. Neuromas, ganglioneuromas, gangliogliomas, ganglioneuroblastomas and neuroblastomas stain positively for neurofilaments. Although typically restricted to neurons, neurofilaments have been detected in paragangliomas and adrenal and extra-adrenal pheochromocytomas. Carcinoids, neuroendocrine carcinomas of the skin, and oat cell carcinomas of the lung also express neurofilaments. For more neurofilament information see Nervous System Cell Type Specific Marker chart online under the CHEMICON Technical Support section.

Egyediség

Strong and specific staining for NF-H with no cross-reactivity for NF-M or NF-L. Reacts with both the phosphorylated and dephosphorylated forms of neurofilament 200 kDa. Stains neurons of the central and peripheral nervous system, including new processes in all organs. Preferentially stains nerve processes.

Immunogén

Epitope: C-terminus
Recombinant fusion protein containing the extreme C-terminus of rat NF-H, prepared from E. coli inclusion bodies by dissolution in urea followed by DEAE-cellulose ion exchange chromatography. Immunogen does not include the lysine-serine-proline

Alkalmazás

Detect Neurofilament H (200 kDa) using this Anti-Neurofilament H (200 kDa) Antibody, C-terminus validated for use in IH & WB.
Immunoblotting

Immunohistochemistry: 1:200

Optimal working dilutions must be determined by end user.
Research Category
Neuroscience
Research Sub Category
Neurofilament & Neuron Metabolism

Neuronal & Glial Markers

Cél megnevezése

200 kDa

Kapcsolódás

Replaces: AB1982

Fizikai forma

Neat rabbit antisera, no preservatives.
Unpurified

Tárolás és stabilitás

Maintain for 1 year at -20°C from date of shipment. Aliquot to avoid repeated freezing and thawing. For maximum recovery of product, centrifuge the original vial after thawing and prior to removing the cap.

Analízis megjegyzés

Control
Brain, Peripheral Nerve

Egyéb megjegyzések

Concentration: Please refer to the Certificate of Analysis for the lot-specific concentration.

Jogi információk

CHEMICON is a registered trademark of Merck KGaA, Darmstadt, Germany

Jogi nyilatkozat

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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Tárolási osztály kódja

10 - Combustible liquids

WGK

WGK 1

Lobbanási pont (F)

Not applicable

Lobbanási pont (C)

Not applicable


Analitikai tanúsítványok (COA)

Analitikai tanúsítványok (COA) keresése a termék sarzs-/tételszámának megadásával. A sarzs- és tételszámok a termék címkéjén találhatók, a „Lot” vagy „Batch” szavak után.

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Az Ön által nemrégiben megvásárolt termékekre vonatkozó dokumentumokat a Dokumentumtárban találja.

Dokumentumtár megtekintése

Thy1.2 YFP-16 transgenic mouse labels a subset of large-diameter sensory neurons that lack TRPV1 expression.
Taylor-Clark, TE; Wu, KY; Thompson, JA; Yang, K; Bahia, PK; Ajmo, JM
Testing null
Karen Ollivier-Lanvin et al.
Experimental neurology, 221(1), 198-205 (2009-11-17)
The H-reflex habituates at relatively low frequency (10 Hz) stimulation in the intact spinal cord, but loss of descending inhibition resulting from spinal cord transection reduces this habituation. There is a return towards a normal pattern of low-frequency habituation in
Mary J Eaton et al.
Neurology research international, 2011, 891605-891605 (2011-07-30)
Transplant of cells which make biologic agents that can modulate the sensory and motor responses after spinal cord injury (SCI) would be useful to treat pain and paralysis. To address this need for clinically useful human cells, a unique neuronal
Yu Zhang et al.
The EMBO journal, 25(24), 5896-5906 (2006-11-25)
Huntington's disease results from a mutation in the HD gene encoding for the protein huntingtin. The function of huntingtin, although beginning to be elucidated, remains largely unclear. To probe the prosurvival function of huntingtin, we modulate levels of wild-type huntingtin
Jean-Luc Boulland et al.
PloS one, 8(8), e71701-e71701 (2013-08-31)
Despite limited regeneration capacity, partial injuries to the adult mammalian spinal cord can elicit variable degrees of functional recovery, mediated at least in part by reorganization of neuronal circuitry. Underlying mechanisms are believed to include synaptic plasticity and collateral sprouting

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