SCG10/Stathmin-2 Antibody [D11B18]

Catalog No.: F4944

Application: Reactivity: Human, Mouse, Rat

サイズ（液体）	価格(税別)	在庫状況
20uL	JPY 25500	国内在庫なし(納期7~10日)
50uL	JPY 42100	国内在庫なし(納期7~10日)
100uL	JPY 63100	国内在庫なし(納期7~10日)
100uL*2	JPY 94700	お問い合わせ

代表番号: 045-509-1970\|電子メール：sales@selleck.co.jp よく尋ねられる質問

使用情報

Dilution

Application
IP, IHC

Source
Mouse Monoclonal Antibody

Reactivity
Human, Mouse, Rat

Storage Buffer
PBS, pH 7.2+50% Glycerol+0.05% BSA+0.01% NaN3

Storage (from the date of receipt)
-20°C (avoid freeze-thaw cycles), 2 years

Predicted MW
˜20 kDa

ポジティブコントロール	Adult rat neocortex; Adult rat hippocampus; Cultured hippocampal neurons (9 DIV)
ネガティブコントロール

プロトコール

IF
Experimental Protocol: Sample Preparation 1. Adherent Cells: Place a clean, sterile coverslip in a culture dish. Once the cells grow to near confluence as a monolayer, remove the coverslip for further use. 2. Suspension Cells: Seed the cells onto a clean, sterile slide coated with poly-L-lysine. 3. Frozen Sections: Allow the slide to thaw at room temperature. Wash it with pure water or PBS for 2 times, 3 minutes each time. 4. Paraffin Sections: Deparaffinization and rehydration. Wash the slide with pure water or PBS for 3 times, 3 minutes each time. Then perform antigen retrieval. Fixation 1. Fix the cell coverslips/spots or tissue sections at room temperature using a fixative such as 4% paraformaldehyde (4% PFA) for 10-15 minutes. 2. Wash the sample with PBS for 3 times, 3 minutes each time. Permeabilization 1.Add a detergent such as 0.1–0.3% Triton X-100 to the sample and incubate at room temperature for 10–20 minutes. (Note: This step is only required for intracellular antigens. For antigens expressed on the cell membrane, this step is unnecessary.) Wash the sample with PBS for 3 times, 3 minutes each time. Blocking Add blocking solution and incubate at room temperature for at least 1 hour. (Common blocking solutions include: serum from the same source as the secondary antibody, BSA, or goat serum.) Note: Ensure the sample remains moist during and after the blocking step to prevent drying, which can lead to high background. Immunofluorescence Staining (Day 1) 1. Remove the blocking solution and add the diluted primary antibody. 2. Incubate the sample in a humidified chamber at 4°C overnight. Immunofluorescence Staining (Day 2) 1. Remove the primary antibody and wash with PBST for 3 times, 5 minutes each time. 2. Add the diluted fluorescent secondary antibody and incubate in the dark at 4°C for 1–2 hours. 3. Remove the secondary antibody and wash with PBST for 3 times, 5 minutes each time. 4. Add diluted DAPI and incubate at room temperature in the dark for 5–10 minutes. 5. Wash with PBST for 3 times, 5 minutes each time. Mounting 1. Mount the sample with an anti-fade mounting medium. 2. Allow the slide to dry at room temperature overnight in the dark. 3. Store the slide in a slide storage box at 4°C, protected from light.

Experimental Protocol:

Sample Preparation

1. Adherent Cells: Place a clean, sterile coverslip in a culture dish. Once the cells grow to near confluence as a monolayer, remove the coverslip for further use.

2. Suspension Cells: Seed the cells onto a clean, sterile slide coated with poly-L-lysine.

3. Frozen Sections: Allow the slide to thaw at room temperature. Wash it with pure water or PBS for 2 times, 3 minutes each time.

4. Paraffin Sections: Deparaffinization and rehydration. Wash the slide with pure water or PBS for 3 times, 3 minutes each time. Then perform antigen retrieval.

Fixation

1. Fix the cell coverslips/spots or tissue sections at room temperature using a fixative such as 4% paraformaldehyde (4% PFA) for 10-15 minutes.

2. Wash the sample with PBS for 3 times, 3 minutes each time.

Permeabilization

1.Add a detergent such as 0.1–0.3% Triton X-100 to the sample and incubate at room temperature for 10–20 minutes.

(Note: This step is only required for intracellular antigens. For antigens expressed on the cell membrane, this step is unnecessary.)

Wash the sample with PBS for 3 times, 3 minutes each time.

Blocking

Add blocking solution and incubate at room temperature for at least 1 hour. (Common blocking solutions include: serum from the same source as the secondary antibody, BSA, or goat serum.)

Note: Ensure the sample remains moist during and after the blocking step to prevent drying, which can lead to high background.

Immunofluorescence Staining (Day 1)

1. Remove the blocking solution and add the diluted primary antibody.

2. Incubate the sample in a humidified chamber at 4°C overnight.

Immunofluorescence Staining (Day 2)

1. Remove the primary antibody and wash with PBST for 3 times, 5 minutes each time.

2. Add the diluted fluorescent secondary antibody and incubate in the dark at 4°C for 1–2 hours.

3. Remove the secondary antibody and wash with PBST for 3 times, 5 minutes each time.

4. Add diluted DAPI and incubate at room temperature in the dark for 5–10 minutes.

5. Wash with PBST for 3 times, 5 minutes each time.

Mounting

1. Mount the sample with an anti-fade mounting medium.

2. Allow the slide to dry at room temperature overnight in the dark.

3. Store the slide in a slide storage box at 4°C, protected from light.

IHC
Experimental Protocol： Deparaffinization/Rehydration 1. Deparaffinize/hydrate sections: 2. Incubate sections in three washes of xylene for 5 min each. 3. Incubate sections in two washes of 100% ethanol for 10 min each. 4. Incubate sections in two washes of 95% ethanol for 10 min each. 5. Wash sections two times in dH2O for 5 min each. 6.Antigen retrieval: For Citrate: Heat slides in a microwave submersed in 1X citrate unmasking solution until boiling is initiated; continue with 10 min at a sub-boiling temperature (95°-98°C). Cool slides on bench top for 30 min. Staining 1. Wash sections in dH2O three times for 5 min each. 2. Incubate sections in 3% hydrogen peroxide for 10 min. 3. Wash sections in dH2O two times for 5 min each. 4. Wash sections in wash buffer for 5 min. 5. Block each section with 100–400 µl of blocking solution for 1 hr at room temperature. 6. Remove blocking solution and add 100–400 µl primary antibody diluent in to each section. Incubate overnight at 4°C. 7. Remove antibody solution and wash sections with wash buffer three times for 5 min each. 8. Cover section with 1–3 drops HRPas needed. Incubate in a humidified chamber for 30 min at room temperature. 9. Wash sections three times with wash buffer for 5 min each. 10. Add DAB Chromogen Concentrate to DAB Diluent and mix well before use. 11. Apply 100–400 µl DAB to each section and monitor closely. 1–10 min generally provides an acceptable staining intensity. 12. Immerse slides in dH2O. 13. If desired, counterstain sections with hematoxylin. 14. Wash sections in dH2O two times for 5 min each. 15. Dehydrate sections: Incubate sections in 95% ethanol two times for 10 sec each; Repeat in 100% ethanol, incubating sections two times for 10 sec each; Repeat in xylene, incubating sections two times for 10 sec each. 16. Mount sections with coverslips and mounting medium.

IHC

Experimental Protocol：

Deparaffinization/Rehydration

1. Deparaffinize/hydrate sections:

2. Incubate sections in three washes of xylene for 5 min each.

3. Incubate sections in two washes of 100% ethanol for 10 min each.

4. Incubate sections in two washes of 95% ethanol for 10 min each.

5. Wash sections two times in dH2O for 5 min each.

6.Antigen retrieval: For Citrate: Heat slides in a microwave submersed in 1X citrate unmasking solution until boiling is initiated; continue with 10 min at a sub-boiling temperature (95°-98°C). Cool slides on bench top for 30 min.

Staining

1. Wash sections in dH2O three times for 5 min each.

2. Incubate sections in 3% hydrogen peroxide for 10 min.

3. Wash sections in dH2O two times for 5 min each.

4. Wash sections in wash buffer for 5 min.

5. Block each section with 100–400 µl of blocking solution for 1 hr at room temperature.

6. Remove blocking solution and add 100–400 µl primary antibody diluent in to each section. Incubate overnight at 4°C.

7. Remove antibody solution and wash sections with wash buffer three times for 5 min each.

8. Cover section with 1–3 drops HRPas needed. Incubate in a humidified chamber for 30 min at room temperature.

9. Wash sections three times with wash buffer for 5 min each.

10. Add DAB Chromogen Concentrate to DAB Diluent and mix well before use.

11. Apply 100–400 µl DAB to each section and monitor closely. 1–10 min generally provides an acceptable staining intensity.

12. Immerse slides in dH2O.

13. If desired, counterstain sections with hematoxylin.

14. Wash sections in dH2O two times for 5 min each.

15. Dehydrate sections: Incubate sections in 95% ethanol two times for 10 sec each; Repeat in 100% ethanol, incubating sections two times for 10 sec each; Repeat in xylene, incubating sections two times for 10 sec each.

16. Mount sections with coverslips and mounting medium.

Datasheet & SDS

生物学的記述

Specificity
SCG10/Stathmin-2 Antibody [D11B18] detects endogenous levels of total SCG10/Stathmin-2 protein.

タンパク質の局在
細胞突起、細胞質、エンドソーム、ゴルジ装置、細胞内膜系

Uniprot ID
Q93045

Clone
D11B18

Synonym(s)
Stathmin-2; Superior cervical ganglion-10 protein (Protein SCG10); Stmn2; Scg10; Scgn10

Background
SCG10 (Stathmin-2, STMN2) is a neuronally enriched microtubule destabilizing protein belonging to the stathmin family, essential for axonal outgrowth and regeneration. It contains an N-terminal regulatory domain with four key phosphorylation sites (Ser22, Ser25, Ser38, Ser63) that are targeted by kinases such as JNK1, MAPK, and PKA. The C-terminal region features an α-helical stathmin-like domain housing two tubulin-binding pockets, enabling SCG10 to sequester α/β-tubulin heterodimers in a 1:2 stoichiometry. This sequestration prevents longitudinal protofilament assembly and thus inhibits microtubule polymerization. In its dephosphorylated state, SCG10 binds free tubulin with high affinity (Kd ~0.3–1 μM), promoting microtubule catastrophe by shifting dynamics toward depolymerization through trapping GTPase-competent tubulin. Phosphorylation of SCG10, however, introduces negative charges and induces conformational changes that disrupt tubulin binding, thereby releasing tubulin heterodimers for microtubule growth. This mechanism stabilizes axonal microtubules during outgrowth. JNK1-mediated phosphorylation of Ser22/Thr22 is particularly important during cortical neuron migration, governing the transition from multipolar to bipolar morphology and modulating the speed of radial migration. SCG10 expression is highest in developing CNS neurons, where it mediates Ca²⁺-dependent microtubule remodeling via calmyrin binding, facilitating growth cone dynamics and contributing to axon regeneration following injury. Loss of TDP-43 in ALS/FTD leads to cryptic exon inclusion in STMN2 transcripts, resulting in depletion of functional SCG10 protein. This causes axonal degeneration, neuromuscular junction retraction, and motor deficits, phenotypes that can be reversed by restoring full-length STMN2 expression.

Background

SCG10 (Stathmin-2, STMN2) is a neuronally enriched microtubule destabilizing protein belonging to the stathmin family, essential for axonal outgrowth and regeneration. It contains an N-terminal regulatory domain with four key phosphorylation sites (Ser22, Ser25, Ser38, Ser63) that are targeted by kinases such as JNK1, MAPK, and PKA. The C-terminal region features an α-helical stathmin-like domain housing two tubulin-binding pockets, enabling SCG10 to sequester α/β-tubulin heterodimers in a 1:2 stoichiometry. This sequestration prevents longitudinal protofilament assembly and thus inhibits microtubule polymerization. In its dephosphorylated state, SCG10 binds free tubulin with high affinity (Kd ~0.3–1 μM), promoting microtubule catastrophe by shifting dynamics toward depolymerization through trapping GTPase-competent tubulin. Phosphorylation of SCG10, however, introduces negative charges and induces conformational changes that disrupt tubulin binding, thereby releasing tubulin heterodimers for microtubule growth. This mechanism stabilizes axonal microtubules during outgrowth. JNK1-mediated phosphorylation of Ser22/Thr22 is particularly important during cortical neuron migration, governing the transition from multipolar to bipolar morphology and modulating the speed of radial migration. SCG10 expression is highest in developing CNS neurons, where it mediates Ca²⁺-dependent microtubule remodeling via calmyrin binding, facilitating growth cone dynamics and contributing to axon regeneration following injury. Loss of TDP-43 in ALS/FTD leads to cryptic exon inclusion in STMN2 transcripts, resulting in depletion of functional SCG10 protein. This causes axonal degeneration, neuromuscular junction retraction, and motor deficits, phenotypes that can be reversed by restoring full-length STMN2 expression.

References
[1] Thornburg-Suresh EJC, et al. J Biol Chem. 2023 Jul;299(7):104861. [2] Thornburg-Suresh EJC, et al. J Neurosci Res. 2024 Sep;102(9):e25382.

PVDFメンブレン孔径参考表

Protein Size (kDa)	PVDF Transfer Membrane Pore Size (μm)
< 10	0.22
10-20	0.22
20-30	0.45
30-45	0.45
45-70	0.45
80-100	0.45
100-140	0.45
> 140	0.45

技術サポート

ストックの作り方、阻害剤の保管方法、細胞実験や動物実験の際に注意すべき点など、製品を取扱う時に問い合わせが多かった質問に対しては取扱説明書でお答えしています。

Handling Instructions

他に質問がある場合は、お気軽にお問い合わせください。

* 必須

* 大学・企業名 大学・企業名を記入してください

* 名前 名前を記入してください

* 電子メール 電子メール・アドレスを記入してください 有効なメールアドレスを入力してください

電話番号

* 内容 お問い合わせ内容をご入力ください

Protein Size (kDa)	Separating Gel Percentage
4-40	20%
12-45	15%
10-70	12.5%
15-100	10%
25-100	8%
60-210	5%