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Merck
모든 사진(2)

주요 문서

N5139

Sigma-Aldrich

Monoclonal Anti-Neurofilament 68 antibody produced in mouse

clone NR4, ascites fluid

동의어(들):

Monoclonal Anti-Neurofilament light chain

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About This Item

MDL number:
UNSPSC 코드:
12352203
NACRES:
NA.41

생물학적 소스

mouse

Quality Level

결합

unconjugated

항체 형태

ascites fluid

항체 생산 유형

primary antibodies

클론

NR4, monoclonal

분자량

antigen apparent mol wt 68 kDa

포함

15 mM sodium azide as preservative

종 반응성

chicken, rat, pig, human

기술

immunohistochemistry (formalin-fixed, paraffin-embedded sections): 1:40 using rat cerebellum
microarray: suitable
western blot: 1:500 using bovine spinal cord neurofilament

동형

IgG1

UniProt 수납 번호

배송 상태

dry ice

저장 온도

−20°C

타겟 번역 후 변형

unmodified

유전자 정보

human ... NEFL(4747)

일반 설명

Monclonal Anti-Neurofilament 68 (mouse IgG1 isotype) is produced by the fusion mouse myeloma cells and splenocytes from an immunized mouse. Neurofilaments are composed of three sub-units- light NFL protein, medium NFM protein, heavy NFH protein. Along with there two other intermediate filaments are present α-internexin and peripherin. Neurofilaments are phosphoproteins. The neurofilaments are one of the five major groups of IFs and are found predominantly in cells or tissues of neuronal origin. They are composed of three major proteins of apparent molecular weights 68 kD, 95kD, and 115kD. Neurofilament proteins are synthesized in the neuronal perikarya, assembled to form filaments and then slowly transported within the axons towards the synaptic terminals.

특이성

The antibody reacts specifically with neurofilament 68 in cultured cells or tissue preparations originating from human, pig, rat or chicken. It does not cross react with other intermediate filament proteins.

면역원

pig spinal cord.

애플리케이션

Monoclonal Anti-Neurofilament 68 antibody has been used:
  • in immunohistochemistry
  • in immunoblotting
  • in western blotting

Mouse Monoclonal clone NR4 anti-Neurofilament 68 antibody may be used for the localization of the neurofilament of molecular weight equal to 68,000 while being non-reactive with other intermediate filament proteins.

생화학적/생리학적 작용

Neurofilaments undergo post-translational modification, which results in their heterogeneity, including different levels of phosphorylation. The phosphorylation of neurofilament polypeptides has been suggested to modulate their function by influencing the interaction between neurofilament and cytoplasmic organelles. Neurofilaments play a role in axonal calibre as they help in movement of an impulse down the axon. Their activity depends on phosphorylation of neurofilaments.Mutations of neurofilaments causes Charcot-Marie-Tooth (CMT) disease. Accumulation of neurofilaments has been observed in many human neurological diseases like Alzheimer′s disease, progressive supranuclear palsy, diabetic neuropathy, and giant axonal neuropathy.

면책조항

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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Storage Class Code

12 - Non Combustible Liquids

WGK

WGK 1

Flash Point (°F)

Not applicable

Flash Point (°C)

Not applicable


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문서 라이브러리 방문

Neurofilament protein synthesis and phosphorylation
Grant P and Pant H C
Journal of Neurocytology, 29(11-12), 843-872 (2000)
Calcium-mediated proteolytic damage in white matter of hydrocephalic rats?
Del Bigio M R.
Journal of Neuropathology and Experimental Neurology, 59(11), 946-954 (2000)
Dorothea Stiefel et al.
Journal of neurosurgery, 99(2 Suppl), 206-213 (2003-09-06)
Tethering of the spinal cord is a well-known complication in humans with spina bifida aperta or occulta. Its pathogenesis consists of a pathological fixation of the spinal cord resulting in traction on the neural tissue which, in turn, leads to
Myoung Sup Shim et al.
Scientific reports, 6, 33830-33830 (2016-09-23)
Mutations in optineurin (OPTN) are linked to the pathology of primary open angle glaucoma (POAG) and amyotrophic lateral sclerosis. Emerging evidence indicates that OPTN mutation is involved in accumulation of damaged mitochondria and defective mitophagy. Nevertheless, the role played by
Expression of peripherin in ubiquinated inclusions of amyotrophic lateral sclerosis
He C Z and Hays A P
Journal of the Neurological Sciences, 217(1), 47-54 (2004)

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