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Bik Recombinant Rabbit Monoclonal Antibody [PSH11-51] - BSA and Azide free

Usd: 649

Specification

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Catalog# HA751413

Bik Recombinant Rabbit Monoclonal Antibody [PSH11-51] - BSA and Azide free

Application

  • WB

  • IF-Cell

  • IP

Reactivity

  • Human

With BSA and Azide
Conjugation

  • unconjugated

Overview

Product Name

Bik Recombinant Rabbit Monoclonal Antibody [PSH11-51] - BSA and Azide free

Antibody Type

Recombinant Rabbit monoclonal Antibody

Immunogen

Recombinant protein within human Bik aa 1-160.

Species Reactivity

Human

Validated Applications

WB, IF-Cell, IP

Target Molecular Weight

Predicted band size: 18 kDa

Positive Control

Ramos cell lysate, Raji cell lysate, THP-1 cell lysate, Ramos.

Conjugation

unconjugated

Clone Number

PSH11-51

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

Bcl-2-interacting killer is a protein that in humans is encoded by the BIK gene. The protein encoded by this gene is known to interact with cellular and viral survival-promoting proteins, such as BCL2 and the Epstein–Barr virus in order to enhance programmed cell death. Because its activity is suppressed in the presence of survival-promoting proteins, this protein is suggested as a likely target for antiapoptotic proteins. This protein shares a critical BH3 domain with other death-promoting proteins, BAX and BAK.

Background References

1. Mebratu YA et al. Bik promotes proteasomal degradation to control low-grade inflammation. J Clin Invest. 2023 Dec

2. Zhang P et al. TMEM215 Prevents Endothelial Cell Apoptosis in Vessel Regression by Blunting BIK-Regulated ER-to-Mitochondrial Ca Influx. Circ Res. 2023 Oct

Subcellular Location

Endomembrane system, Mitochondrion membrane.

UNIPROT

SwissProt: Q13323 Human

Synonyms

Apoptosis inducer NBK antibody

BBC1 antibody

Bcl-2-interacting killer antibody

BCL2 interacting killer antibody

bhikhari antibody

BIK antibody

Bik-like killer protein antibody

BIK_HUMAN antibody

BIP 1 antibody

BiP1 antibody

Expand

Images

  • <span style="font-weight: bold;">☑ Relative expression (RE)</span><br /><br />This data was developed using <a href="/products/HA723343" style="font-weight: bold;text-decoration: underline;">HA723343</a>, the same antibody clone in a different buffer formulation.<br />Western blot analysis of Bik on different lysates with Rabbit anti-Bik antibody (<a href="/products/HA723343" style="font-weight: bold;text-decoration: underline;">HA723343</a>) at 1/10,000 dilution.<br /><br />Lane 1: Ramos cell lysate<br />Lane 2: SK-Br-3 cell lysate (negative)<br />Lane 3: Raji cell lysate<br />Lane 4: THP-1 cell lysate<br /><br />Lysates/proteins at 20 µg/Lane.<br /><br />Predicted band size: 18 kDa<br />Observed band size: 18 kDa<br /><br />Exposure time: 25 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/HA723343" style="font-weight: bold;text-decoration: underline;">HA723343</a>) at 1/10,000 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 HA723343, the same antibody clone in a different buffer formulation.
    Western blot analysis of Bik on different lysates with Rabbit anti-Bik antibody (HA723343) at 1/10,000 dilution.

    Lane 1: Ramos cell lysate
    Lane 2: SK-Br-3 cell lysate (negative)
    Lane 3: Raji cell lysate
    Lane 4: THP-1 cell lysate

    Lysates/proteins at 20 µg/Lane.

    Predicted band size: 18 kDa
    Observed band size: 18 kDa

    Exposure time: 25 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 (HA723343) at 1/10,000 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.

  • This data was developed using <a href="/products/HA723343" style="font-weight: bold;text-decoration: underline;">HA723343</a>, the same antibody clone in a different buffer formulation.<br />Immunocytochemistry analysis of Ramos cells labeling Bik with Rabbit anti-Bik antibody (<a href="/products/HA723343" style="font-weight: bold;text-decoration: underline;">HA723343</a>) at 1/100 dilution.<br /><br />Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 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-Bik antibody (<a href="/products/HA723343" style="font-weight: bold;text-decoration: underline;">HA723343</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/HA601187" style="font-weight: bold;text-decoration: underline;">HA601187</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.

    This data was developed using HA723343, the same antibody clone in a different buffer formulation.
    Immunocytochemistry analysis of Ramos cells labeling Bik with Rabbit anti-Bik antibody (HA723343) at 1/100 dilution.

    Cells were fixed in 4% paraformaldehyde for 15 minutes at room temperature, permeabilized with 0.1% Triton X-100 in PBS for 15 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-Bik antibody (HA723343) 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 (HA601187, 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/HA723343" style="font-weight: bold;text-decoration: underline;">HA723343</a>, the same antibody clone in a different buffer formulation.<br />Bik was immunoprecipitated from 0.2 mg Ramos cell lysate with <a href="/products/HA723343" style="font-weight: bold;text-decoration: underline;">HA723343</a> at 2 µg/10 µl beads. Western blot was performed from the immunoprecipitate using <a href="/products/HA723343" style="font-weight: bold;text-decoration: underline;">HA723343</a> at 1/1,000 dilution. HRP Conjugated Anti-Rabbit IgG for IP Nano-secondary antibody at 1/5,000 dilution was used for 1 hour at room temperature.<br /><br />Lane 1: Ramos cell lysate (input)<br />Lane 2: <a href="/products/HA723343" style="font-weight: bold;text-decoration: underline;">HA723343</a> IP in Ramos cell lysate<br />Lane 3: Rabbit IgG instead of <a href="/products/HA723343" style="font-weight: bold;text-decoration: underline;">HA723343</a> in Ramos cell lysate<br /><br />Blocking/Dilution buffer: 5% NFDM/TBST<br />Exposure time: 20 seconds; ECL: <a href="/products/K1801" style="font-weight: bold;text-decoration: underline;">K1801</a>

    This data was developed using HA723343, the same antibody clone in a different buffer formulation.
    Bik was immunoprecipitated from 0.2 mg Ramos cell lysate with HA723343 at 2 µg/10 µl beads. Western blot was performed from the immunoprecipitate using HA723343 at 1/1,000 dilution. HRP Conjugated Anti-Rabbit IgG for IP Nano-secondary antibody at 1/5,000 dilution was used for 1 hour at room temperature.

    Lane 1: Ramos cell lysate (input)
    Lane 2: HA723343 IP in Ramos cell lysate
    Lane 3: Rabbit IgG instead of HA723343 in Ramos cell lysate

    Blocking/Dilution buffer: 5% NFDM/TBST
    Exposure time: 20 seconds; ECL: K1801

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