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SOX10 Recombinant Rabbit Monoclonal Antibody [PDH0-03]

Usd: 385

Specification

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Catalog# HA721240

SOX10 Recombinant Rabbit Monoclonal Antibody [PDH0-03]

Application

  • WB

  • IHC-P

  • IF-Cell

  • IF-Tissue

  • FC

  • IHC-Fr

  • IP

Reactivity

  • Human

  • Mouse

  • Rat

Predicted reactivity

  • Cynomolgus monkey

  • Pig

Predicted species support after-sales service
Conjugation

  • unconjugated

Overview

Product Name

SOX10 Recombinant Rabbit Monoclonal Antibody [PDH0-03]

Antibody Type

Recombinant Rabbit monoclonal Antibody

Immunogen

Synthetic peptide within C terminal human SOX10.

Species Reactivity

Human, Mouse, Rat (Predicted: Cynomolgus monkey, Pig)

Predicted species support after-sales service

Validated Applications

WB, IHC-P, IF-Cell, IF-Tissue, FC, IHC-Fr, IP

Molecular Weight

Predicted band size: 50 kDa

Positive Control

Mouse brain tissue, mouse cerebellum tissue, rat cerebellum tissue, human breast tissue, human malignant melanoma tissue, A375 cell lysate, B16-F1 cell lysate, C6 cell lysate, A375, B16F1.

Conjugation

unconjugated

Clone Number

PDH0-03

RRID

AB_3072360

Product Features

Form

Liquid

Concentration

Storage Instructions

Shipped at 4℃. Store at +4℃ short term (1-2 weeks). It is recommended to aliquot into single-use upon delivery. Store at -20℃ long term.

Storage Buffer

PBS (pH7.4), 0.1% BSA, 40% Glycerol. Preservative: 0.05% Sodium Azide.

Isotype

IgG

Purification Method

Protein A affinity purified.

Application Dilution

  • WB

  • 1:1,000-1:2,000

  • IHC-P

  • 1:1,000-1:3,000

  • IF-Cell

  • 1:50

  • IF-Tissue

  • 1:500

  • FC

  • 1:500-1:1,000

  • IHC-Fr

  • 1:500-1:1,000

  • IP

  • 1-2μg/sample

Target

Function

SOX10 is a neural crest transcription factor crucial for specification, maturation, and maintenance of Schwann cells and melanocytes. SOX10 is involved in the generation of myelin through interaction with OLIG1. In melanocytic cells the SOX10 gene expression is regulated by microphtalmia transcription factor. The SOX10 nuclear protein is widely expressed in glial cells, Schwann cells, and myoepithelial cells (salivary, bronchial, and mammary glands). SOX10 is expressed in virtually all cases of naevus and malignant melanoma (including 97-100% of desmoplastic and spindle cell melanomas), schwannoma, neurofibroma and granular cell tumour. SOX10 is expressed in the majority of cases of oligodendroglioma, astrocytoma and glioblastoma (few studies), desmoplastic/triple-negative breast carcinoma, acinic cell carcinoma, adenoid cystic carcinoma, epithelial-myoepithelial and myoepithelial carcinoma, and pleomorphic adenoma component of salivary gland adenocarcinoma. SOX10 is expressed in about half of cases of malignant nerve sheath tumour, and clear cell sarcoma (tendons and aponeuroses). Rare cases of luminal type breast ductal carcinoma and synovial sarcoma have shown SOX10 positivity. Apart from the above mentioned, epithelial and mesenchymal tumours are uniformly SOX10 negative. In paragangliomas/phaeochromocytomas and epithelial neuroendocrine tumours, SOX10 is only expressed in sustentacular cells but not in tumour cells. SOX10 is more specific than S100 protein in the detection of melanocytic and schwannian neoplasms, and has in some studies shown more sensitive. Skin and colon/appendix are recommended as positive and negative tissue controls for SOX10. In skin, moderate to strong nuclear staining reaction in virtually all melanocytes must be seen. The vast majority of myoepithelial cells lining sweat glands must show an at least moderate nuclear staining reaction. In colon/appendix, virtually all Schwann cells must display an as strong as possible nuclear staining reaction without any staining reaction of epithelial cells and smooth muscle cells. At present, and as specified in previous assessments, no reliable tissue component with consistent low level expression of SOX10 has been identified, monitoring the overall analytical sensitivity of an assay. Due to this issue both skin and colon/appendix are needed as tissue controls for SOX10.

Background References

1. Pingault V et al. SOX10: 20 years of phenotypic plurality and current understanding of its developmental function. J Med Genet. 2022 Feb

2. Yoon EC et al. TRPS1, GATA3, and SOX10 expression in triple-negative breast carcinoma. Hum Pathol. 2022 Jul

Subcellular Location

Cytoplasm, Nucleus, Mitochondrion outer membrane.

UNIPROT

SwissProt: P56693 Human

SwissProt: Q04888 Mouse

SwissProt: O55170 Rat

Synonyms

DOM antibody

DOM antibody

Dominant megacolon mouse human homolog of antibody

MGC15649 antibody

PCWH antibody

SOX 10 antibody

SOX10 antibody

SOX10_HUMAN antibody

SRY (sex determining region Y) box 10 antibody

SRY (sex determining region Y) box 10 antibody

Expand

Images

  • Application: IHC-Fr<br /><br />Species: Mouse<br /><br />Site: Cerebellum <br /><br />Sample: Frozen section<br /><br />Antibody concentration: 1: 1,000<br /><br />Antigen retrieval: Not required

    Application: IHC-Fr

    Species: Mouse

    Site: Cerebellum

    Sample: Frozen section

    Antibody concentration: 1: 1,000

    Antigen retrieval: Not required

  • Application: IHC-Fr<br /><br />Species: Mouse<br /><br />Site: Cerebral cortex<br /><br />Sample: Frozen section<br /><br />Antibody concentration: 1: 500<br /><br />Antigen retrieval: Not required

    Application: IHC-Fr

    Species: Mouse

    Site: Cerebral cortex

    Sample: Frozen section

    Antibody concentration: 1: 500

    Antigen retrieval: Not required

  • Application: IHC-Fr<br /><br />Species: Rat<br /><br />Site: Cerebellum <br /><br />Sample: Frozen section<br /><br />Antibody concentration: 1: 500<br /><br />Antigen retrieval: Not required

    Application: IHC-Fr

    Species: Rat

    Site: Cerebellum

    Sample: Frozen section

    Antibody concentration: 1: 500

    Antigen retrieval: Not required

  • Immunohistochemical analysis of paraffin-embedded mouse brain tissue with Rabbit anti-SOX10 antibody (<a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a>) at 1/1,000 dilution.<br /><br />The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH<sub>2</sub>O and PBS, and then probed with the primary antibody (<a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a>) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

    Immunohistochemical analysis of paraffin-embedded mouse brain tissue with Rabbit anti-SOX10 antibody (HA721240) at 1/1,000 dilution.

    The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721240) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

  • Immunohistochemical analysis of paraffin-embedded mouse cerebellum tissue with Rabbit anti-SOX10 antibody (<a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a>) at 1/1,000 dilution.<br /><br />The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH<sub>2</sub>O and PBS, and then probed with the primary antibody (<a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a>) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

    Immunohistochemical analysis of paraffin-embedded mouse cerebellum tissue with Rabbit anti-SOX10 antibody (HA721240) at 1/1,000 dilution.

    The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721240) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

  • Immunohistochemical analysis of paraffin-embedded rat cerebellum tissue with Rabbit anti-SOX10 antibody (<a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a>) at 1/1,000 dilution.<br /><br />The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH<sub>2</sub>O and PBS, and then probed with the primary antibody (<a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a>) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

    Immunohistochemical analysis of paraffin-embedded rat cerebellum tissue with Rabbit anti-SOX10 antibody (HA721240) at 1/1,000 dilution.

    The section was pre-treated using heat mediated antigen retrieval with Tris-EDTA buffer (pH 9.0) for 20 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721240) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

  • Immunohistochemical analysis of paraffin-embedded human breast tissue with Rabbit anti-SOX10 antibody (<a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a>) at 1/1,000 dilution.<br /><br />The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH<sub>2</sub>O and PBS, and then probed with the primary antibody (<a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a>) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

    Immunohistochemical analysis of paraffin-embedded human breast tissue with Rabbit anti-SOX10 antibody (HA721240) at 1/1,000 dilution.

    The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721240) at 1/1,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

  • Immunohistochemical analysis of paraffin-embedded human malignant melanoma tissue with Rabbit anti-SOX10 antibody (<a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a>) at 1/3,000 dilution.<br /><br />The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH<sub>2</sub>O and PBS, and then probed with the primary antibody (<a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a>) at 1/3,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

    Immunohistochemical analysis of paraffin-embedded human malignant melanoma tissue with Rabbit anti-SOX10 antibody (HA721240) at 1/3,000 dilution.

    The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721240) at 1/3,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

  • <span style="font-weight: bold;">☑ Relative expression (RE)</span><br /><br />Immunohistochemical analysis of paraffin-embedded human kidney tissue (Negative control) with Rabbit anti-SOX10 antibody (<a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a>) at 1/3,000 dilution.<br /><br />The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH<sub>2</sub>O and PBS, and then probed with the primary antibody (<a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a>) at 1/3,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

    ☑ Relative expression (RE)

    Immunohistochemical analysis of paraffin-embedded human kidney tissue (Negative control) with Rabbit anti-SOX10 antibody (HA721240) at 1/3,000 dilution.

    The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721240) at 1/3,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

  • <span style="font-weight: bold;">☑ Relative expression (RE)</span><br /><br />Immunohistochemical analysis of paraffin-embedded human esophagus tissue (Negative control) with Rabbit anti-SOX10 antibody (<a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a>) at 1/3,000 dilution.<br /><br />The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH<sub>2</sub>O and PBS, and then probed with the primary antibody (<a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a>) at 1/3,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

    ☑ Relative expression (RE)

    Immunohistochemical analysis of paraffin-embedded human esophagus tissue (Negative control) with Rabbit anti-SOX10 antibody (HA721240) at 1/3,000 dilution.

    The section was pre-treated using heat mediated antigen retrieval with sodium citrate buffer (pH 6.0) (high pressure) for 2 minutes. The tissues were blocked in 1% BSA for 20 minutes at room temperature, washed with ddH2O and PBS, and then probed with the primary antibody (HA721240) at 1/3,000 dilution for 1 hour at room temperature. The detection was performed using an HRP conjugated compact polymer system. DAB was used as the chromogen. Tissues were counterstained with hematoxylin and mounted with DPX.

  • Western blot analysis of SOX10 on different lysates with Rabbit anti-SOX10 antibody (<a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a>) at 1/1,000 dilution.<br /><br />Lane 1: A375 cell lysate<br />Lane 2: B16-F1 cell lysate<br />Lane 3: C6 cell lysate<br /><br />Lysates/proteins at 20 µg/Lane.<br /><br />Predicted band size: 50 kDa<br />Observed band size: 60-75 kDa<br /><br />Exposure time: 4 seconds; ECL: K1801;<br /><br />4-20% SDS-PAGE gel.<br /><br />Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (<a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a>) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (<a href="/products/HA1001" style="font-weight: bold;text-decoration: underline;">HA1001</a>) at 1/50,000 dilution was used for 1 hour at room temperature.

    Western blot analysis of SOX10 on different lysates with Rabbit anti-SOX10 antibody (HA721240) at 1/1,000 dilution.

    Lane 1: A375 cell lysate
    Lane 2: B16-F1 cell lysate
    Lane 3: C6 cell lysate

    Lysates/proteins at 20 µg/Lane.

    Predicted band size: 50 kDa
    Observed band size: 60-75 kDa

    Exposure time: 4 seconds; ECL: K1801;

    4-20% SDS-PAGE gel.

    Proteins were transferred to a PVDF membrane and blocked with 5% NFDM/TBST for 1 hour at room temperature. The primary antibody (HA721240) at 1/1,000 dilution was used in 5% NFDM/TBST at 4℃ overnight. Goat Anti-Rabbit IgG - HRP Secondary Antibody (HA1001) at 1/50,000 dilution was used for 1 hour at room temperature.

  • Immunocytochemistry analysis of A375 cells labeling SOX10 with Rabbit anti-SOX10 antibody (<a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a>) at 1/50 dilution.<br /><br />Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-SOX10 antibody (<a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a>) at 1/50 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor&trade; 488, <a href="/products/HA1121" style="font-weight: bold;text-decoration: underline;">HA1121</a>) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.

    Immunocytochemistry analysis of A375 cells labeling SOX10 with Rabbit anti-SOX10 antibody (HA721240) at 1/50 dilution.

    Cells were fixed in 4% paraformaldehyde for 10 minutes at 37 ℃, permeabilized with 0.05% Triton X-100 in PBS for 20 minutes, and then blocked with 2% negative goat serum for 30 minutes at room temperature. Cells were then incubated with Rabbit anti-SOX10 antibody (HA721240) at 1/50 dilution in 2% negative goat serum overnight at 4 ℃. Goat Anti-Rabbit IgG H&L (iFluor™ 488, HA1121) was used as the secondary antibody at 1/1,000 dilution. PBS instead of the primary antibody was used as the secondary antibody only control. Nuclear DNA was labelled in blue with DAPI.

  • Flow cytometric analysis of A375 cells labeling SOX10.<br /><br />Cells were fixed and permeabilized. Then stained with the primary antibody (<a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a>, 1ug/ml) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor&trade; 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (<a href="/products/HA1121" style="font-weight: bold;text-decoration: underline;">HA1121</a>) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).

    Flow cytometric analysis of A375 cells labeling SOX10.

    Cells were fixed and permeabilized. Then stained with the primary antibody (HA721240, 1ug/ml) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).

  • Flow cytometric analysis of B16F1 cells labeling SOX10.<br /><br />Cells were fixed and permeabilized. Then stained with the primary antibody (<a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a>, 1ug/ml) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor&trade; 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (<a href="/products/HA1121" style="font-weight: bold;text-decoration: underline;">HA1121</a>) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).

    Flow cytometric analysis of B16F1 cells labeling SOX10.

    Cells were fixed and permeabilized. Then stained with the primary antibody (HA721240, 1ug/ml) (red) compared with Rabbit IgG Isotype Control (green). After incubation of the primary antibody at +4℃ for an hour, the cells were stained with a iFluor™ 488 conjugate-Goat anti-Rabbit IgG Secondary antibody (HA1121) at 1/1,000 dilution for 30 minutes at +4℃. Unlabelled sample was used as a control (cells without incubation with primary antibody; black).

  • SOX10 was immunoprecipitated from 0.2 mg A375 cell lysate with <a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a> at 2 µg/10 µl beads. Western blot was performed from the immunoprecipitate using <a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a> at 1/2,000 dilution. Anti-Rabbit IgG for IP Nano-secondary antibody (NBI01H) at 1/5,000 dilution was used for 1 hour at room temperature.<br /><br />Lane 1: A375 cell lysate (input)<br />Lane 2: <a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a> IP in A375 cell lysate<br />Lane 3: Rabbit IgG instead of <a href="/products/HA721240" style="font-weight: bold;text-decoration: underline;">HA721240</a> in A375 cell lysate<br /><br />Blocking/Dilution buffer: 5% NFDM/TBST<br />Exposure time: 26 seconds; ECL: <a href="/products/K1801" style="font-weight: bold;text-decoration: underline;">K1801</a>

    SOX10 was immunoprecipitated from 0.2 mg A375 cell lysate with HA721240 at 2 µg/10 µl beads. Western blot was performed from the immunoprecipitate using HA721240 at 1/2,000 dilution. Anti-Rabbit IgG for IP Nano-secondary antibody (NBI01H) at 1/5,000 dilution was used for 1 hour at room temperature.

    Lane 1: A375 cell lysate (input)
    Lane 2: HA721240 IP in A375 cell lysate
    Lane 3: Rabbit IgG instead of HA721240 in A375 cell lysate

    Blocking/Dilution buffer: 5% NFDM/TBST
    Exposure time: 26 seconds; ECL: K1801

  • Application: IF-Tissue<br /><br />Species: Mouse<br /><br />Site: brain<br /><br />Sample: Paraffin-embedded section<br /><br />Antibody concentration: 1/500

    Application: IF-Tissue

    Species: Mouse

    Site: brain

    Sample: Paraffin-embedded section

    Antibody concentration: 1/500

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