NE1017

Anti-Pan-Neuronal Neurofilament Marker Mouse mAb (SMI-311)

liquid, clone SMI-311, Calbiochem^®

• UNSPSCコード: 12352203

特性

• 由来生物: mouse
• 品質水準: 100
• 抗体製品の状態: ascites fluid
• 抗体製品タイプ: primary antibodies
• クローン: SMI-311, monoclonal
• 形状: liquid
• 含みます: ≤0.1% sodium azide as preservative
• 化学種の反応性（ホモロジーによる予測）: mammals
• メーカー／製品名: Calbiochem^®
• 保管条件: OK to freeze; avoid repeated freeze/thaw cycles
• アイソタイプ: IgG1, IgGM
• 輸送温度: wet ice
• 保管温度: −20°C
• ターゲットの翻訳後修飾: unmodified
• 遺伝子情報: human ... NEFL(4747)

詳細

詳細

Mouse monoclonal antibody supplied as undiluted ascites. Recognizes the ~180-200 kDa pan-neuronal neurofilament marker protein.

Recognizes ~180-200 kDa pan-neuronal neurofilament marker in rat central nervous system cytoskeletal preparations.

This Anti-Pan-Neuronal Neurofilament Marker Mouse mAb (SMI-311) is validated for use in ELISA, Frozen Sections, WB, ICC, Paraffin Sections for the detection of Pan-Neuronal Neurofilament Marker.

免疫原

Rat

homogenized hypothalami extracted from Fischer 344 rat brain

アプリケーション

ELISA (1:1000)
Frozen Sections (1:1000, see comments)
Immunoblotting (1:1000)
Immunocytochemistry (1:1000, see comments)
Paraffin Sections (1:1000, heat pre-treatment required, see comments)

警告

Toxicity: Standard Handling (A)

物理的形状

Undiluted ascites.

再構成

Following initial thaw, aliquot and freeze (-20°C).

アナリシスノート

Positive Control
Rat brain or rat CNS cytoskeletal preparations

その他情報

Agostino, A., et al. 2003. Hum. Mol. Genet.12, 399.
Tsunoda, I., et al. 2003. Am. J. Pathol.162, 1259.
Ulfig, N., et al. 1998. Cell Tissue Res.291, 433.

This antibody cocktail was selected to provide a specific marker for neurons in tissue sections and cultured cells. In contrast to individual anti-nonphosphoneurofilament antibodies that identify different subsets of neurons, this cocktail is a convenient marker for neurons in general and their differentiation from non-neuronal cells. Also useful as an early marker of neuronal migration and differentiation in human fetal development, yielding Golgi-like images without the disadvantages of the lack of selectivity and poor specificity of the Golgi technique. Can be used to trace the "inside-out gradient" of neuron production and differentiation in specifically delineating cell bodies and dendrites. Certain pathologic conditions, such as malnutrition, affect the SMI-311-visualized soma size and dendritic arborization. Tissues and cultured cells can be fixed in a variety of paraformaldehyde- or formaldehyde-containing fixatives, including Bouin′s fixative. This antibody does not react well with tissues or cells fixed in glutaraldehyde/paraformaldehyde. For staining paraffin sections it is recommended that de-paraffinized tissues be autoclaved in dH₂O for 10 min to expose the epitope. Trypsin pre-treatment will abolish reactivity. Post-fixation in cold methanol or methanol/hydrogen peroxide facilitates access of the antibody to the neurons in frozen sections and thick tissues sections that have been fixed in 4% paraformaldehyde or cultured cells. For tissues that have not been paraffin-embedded and have been stored for long periods of time in formaldehyde fixatives, it is recommended that the tissues (up to 0.5 cm thick) be boiled in Tris-buffered saline, pH 9.0 for 15 min prior to sectioning. Antibody should be titrated for optimal results in individual systems.

法的情報

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

安全性情報

• 保管分類コード: 10 - Combustible liquids
• WGK: WGK 1