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TMEM16A Recombinant Rabbit Monoclonal Antibody [PSH06-56] - BSA and Azide free

Usd: 649

Specification

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Catalog# HA751085

TMEM16A Recombinant Rabbit Monoclonal Antibody [PSH06-56] - BSA and Azide free

Application

  • WB

  • IF-Cell

  • FC

Reactivity

  • Human

With BSA and Azide
Conjugation

  • unconjugated

Overview

Product Name

TMEM16A Recombinant Rabbit Monoclonal Antibody [PSH06-56] - BSA and Azide free

Antibody Type

Recombinant Rabbit monoclonal Antibody

Immunogen

Recombinant protein within human TMEM16A aa 1-333.

Species Reactivity

Human

Validated Applications

WB, IF-Cell, FC

Target Molecular Weight

Predicted band size: 114 kDa

Positive Control

HT-29 cell lysate, HCT 116 cell lysate, BxPC-3 cell lysate, HT-29.

Conjugation

unconjugated

Clone Number

PSH06-56

Product Features

Form

Liquid

Concentration

1mg/ml

Storage Instructions

Store at 2-8℃. Avoid freeze.

Storage Buffer

1*PBS (pH7.4).

Isotype

IgG

Purification Method

Protein A affinity purified.

Application Dilution

Target

Function

Anoctamin-1 (ANO1), also known as Transmembrane member 16A (TMEM16A), is a protein that, in humans, is encoded by the ANO1 gene. Anoctamin-1 is a voltage-gated calcium-activated anion channel, which acts as a chloride channel and a bicarbonate channel. additionally Anoctamin-1 is apical iodide channel. It is expressed in smooth muscle, epithelial cells, vomeronasal neurons, olfactory sustentacular cells, and is highly expressed in interstitial cells of Cajal (ICC) throughout the gastrointestinal tract.

Background References

1. Li S et al. TMEM16A ion channel: A novel target for cancer treatment. Life Sci. 2023 Oct

2. Liu Y et al. The Ca(2+)-activated chloride channel ANO1/TMEM16A: An emerging therapeutic target for epithelium-originated diseases? Acta Pharm Sin B. 2021 Jun

Subcellular Location

Apical cell membrane, Presynapse.

UNIPROT

SwissProt: Q5XXA6 Human

Synonyms

ANO 1 antibody

ANO1 antibody

ANO1_HUMAN antibody

Anoctamin 1 antibody

Anoctamin 1 calcium activated chloride channel antibody

Anoctamin-1 antibody

Anoctamin1 antibody

Ca2+ activated Cl- channel antibody

Calcium Activated Chloride Channel antibody

Discovered on gastrointestinal stromal tumors protein 1 antibody

Expand

Images

  • <span style="font-weight: bold;">☑ Relative expression (RE)</span><br /><br />This data was developed using <a href="/products/HA722720" style="font-weight: bold;text-decoration: underline;">HA722720</a>, the same antibody clone in a different buffer formulation.<br />Western blot analysis of TMEM16A on different lysates with Rabbit anti-TMEM16A antibody (<a href="/products/HA722720" style="font-weight: bold;text-decoration: underline;">HA722720</a>) at 1/1,000 dilution.<br /><br />Lane 1: HT-29 cell lysate<br />Lane 2: HCT 116 cell lysate<br />Lane 3: BxPC-3 cell lysate<br />Lane 4: HeLa cell lysate (negative)<br /><br />Lysates/proteins at 20 µg/Lane.<br /><br />Predicted band size: 114 kDa<br />Observed band size: 150 kDa<br /><br />Exposure time: 10 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/HA722720" style="font-weight: bold;text-decoration: underline;">HA722720</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.

    ☑ Relative expression (RE)

    This data was developed using HA722720, the same antibody clone in a different buffer formulation.
    Western blot analysis of TMEM16A on different lysates with Rabbit anti-TMEM16A antibody (HA722720) at 1/1,000 dilution.

    Lane 1: HT-29 cell lysate
    Lane 2: HCT 116 cell lysate
    Lane 3: BxPC-3 cell lysate
    Lane 4: HeLa cell lysate (negative)

    Lysates/proteins at 20 µg/Lane.

    Predicted band size: 114 kDa
    Observed band size: 150 kDa

    Exposure time: 10 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 (HA722720) 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.

  • <span style="font-weight: bold;">☑ Relative expression (RE)</span><br /><br />This data was developed using <a href="/products/HA722720" style="font-weight: bold;text-decoration: underline;">HA722720</a>, the same antibody clone in a different buffer formulation.<br />Immunocytochemistry analysis of HT-29 (positive) and HeLa (negative) labeling TMEM16A with Rabbit anti-TMEM16A antibody (<a href="/products/HA722720" style="font-weight: bold;text-decoration: underline;">HA722720</a>) at 1/100 dilution.<br /><br />Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-TMEM16A antibody (<a href="/products/HA722720" style="font-weight: bold;text-decoration: underline;">HA722720</a>) at 1/100 dilution in 1% BSA in PBST 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.<br /><br />Beta tubulin (<a href="/products/M1305-2" style="font-weight: bold;text-decoration: underline;">M1305-2</a>, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor&trade; 594, <a href="/products/HA1126" style="font-weight: bold;text-decoration: underline;">HA1126</a>) was used as the secondary antibody at 1/1,000 dilution.

    ☑ Relative expression (RE)

    This data was developed using HA722720, the same antibody clone in a different buffer formulation.
    Immunocytochemistry analysis of HT-29 (positive) and HeLa (negative) labeling TMEM16A with Rabbit anti-TMEM16A antibody (HA722720) at 1/100 dilution.

    Cells were fixed in 4% paraformaldehyde for 20 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 5 minutes at room temperature, then blocked with 1% BSA in 10% negative goat serum for 1 hour at room temperature. Cells were then incubated with Rabbit anti-TMEM16A antibody (HA722720) at 1/100 dilution in 1% BSA in PBST 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.

    Beta tubulin (M1305-2, red) was stained at 1/100 dilution overnight at +4℃. Goat Anti-Mouse IgG H&L (iFluor™ 594, HA1126) was used as the secondary antibody at 1/1,000 dilution.

  • This data was developed using <a href="/products/HA722720" style="font-weight: bold;text-decoration: underline;">HA722720</a>, the same antibody clone in a different buffer formulation.<br />Flow cytometric analysis of HT-29 cells labeling TMEM16A.<br /><br />Cells were fixed and permeabilized. Then stained with the primary antibody (<a href="/products/HA722720" style="font-weight: bold;text-decoration: underline;">HA722720</a>, 1μg/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).

    This data was developed using HA722720, the same antibody clone in a different buffer formulation.
    Flow cytometric analysis of HT-29 cells labeling TMEM16A.

    Cells were fixed and permeabilized. Then stained with the primary antibody (HA722720, 1μg/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).

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"