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BSA Mouse Monoclonal Antibody [A7D11]

Usd: 350

Specification

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Catalog# HA600086

BSA Mouse Monoclonal Antibody [A7D11]

Application

  • ELISA

  • WB

Reactivity

  • Cow

Conjugation

  • unconjugated

Overview

Product Name

BSA Mouse Monoclonal Antibody [A7D11]

Antibody Type

Mouse Monoclonal Antibody

Immunogen

Native protein.

Species Reactivity

Cow

Validated Applications

ELISA, WB

Target Molecular Weight

Predicted band size: 66 kDa

Positive Control

BSA protein.

Conjugation

unconjugated

Clone Number

A7D11

RRID

AB_3071702

Product Features

Form

Liquid

Concentration

2 mg/mL.(The concentration of this product may be batch-dependent)

Storage Instructions

Store at 2-8℃. Avoid freeze.

Storage Buffer

PBS (pH7.4).

Isotype

IgG1

Purification Method

Protein G affinity purified.

Application Dilution

  • ELISA

  • 1:10,000

  • WB

  • 1:500

Target

Function

Bovine serum albumin (BSA) is an abundant plasma protein in cows that is important for maintaining osmotic pressure in blood plasma for proper distribution of body fluids between intravascular compartments and body tissues. BSA is a common buffer component for immunoglobulin type assays due to good solubility characteristics for water, Ca2+, Na+, K+, fatty acids, hormones and bilirubin. BSA makes up about half of the protein in plasma and represents the most stable and soluble protein in the plasma. It is a suitable reagent for laboratories developing immunoassays, mostly due to its availability, solubility and the numerous functional groups present for coupling. The BSA component contains several lysines that are capable of reacting with conjugation sites of linkers, making it applicable as a carrier protein for antigenic compounds. BSA Antibody is a high quality monoclonal BSA antibody (also designated Fraction V antibody, ALB antibody, or Bos Taurus Serum Albumin antibody) suitable for the detection of the BSA protein of bovine origin. Anti-bovine serum albumin (anti-BSA) antibody can be used for the detection of BSA in tracer studies or in protease assays. This antibody demonstrates high specificity for BSA and no crossreactivity to HSA (Human serum albumin), Goat serum and Rabbit serum.

Background References

1. Ambrósio JAR. et. al. BSA nanoparticles loaded-methylene blue for photodynamic antimicrobial chemotherapy (PACT): effect on both growth and biofilm formation by Candida albicans. J Biomater Sci Polym Ed. 2020 Dec

Subcellular Location

Secreted.

UNIPROT

SwissProt: P02769 Bovine

Synonyms

Albumin

BSA

Bos d 6

ALB

Images

  • Bovine Serum Albumin Antibody (<a href="/products/HA600086" style="font-weight: bold;text-decoration: underline;">HA600086</a>) in indirect ELISA.<br /><br />Indirect ELISA analysis of BSA was performed by coating wells of a 96-well plate with 100 µl per well of BSA standard diluted in carbonate/bicarbonate buffer, at a concentration of 1 µg/mL overnight at 4℃. Wells of the plate were washed, blocked with StartingBlock blocking buffer, and incubated with 100 µl per well of a mouse BSA monoclonal antibody starting at a concentration of 20 µg/mL and serially diluting it to a concentration of 1.28 ng/mL for 2 hours at room temperature. The plate was washed and incubated with 100 µl per well of an HRP-conjugated goat anti-mouse IgG secondary antibody at a dilution of 1:10,000 for one hour at room temperature. Detection was performed using an Ultra TMB Substrate for 5 minutes at room temperature in the dark. The reaction was stopped with sulfuric acid and absorbances were read on a spectrophotometer at 450 nm.

    Bovine Serum Albumin Antibody (HA600086) in indirect ELISA.

    Indirect ELISA analysis of BSA was performed by coating wells of a 96-well plate with 100 µl per well of BSA standard diluted in carbonate/bicarbonate buffer, at a concentration of 1 µg/mL overnight at 4℃. Wells of the plate were washed, blocked with StartingBlock blocking buffer, and incubated with 100 µl per well of a mouse BSA monoclonal antibody starting at a concentration of 20 µg/mL and serially diluting it to a concentration of 1.28 ng/mL for 2 hours at room temperature. The plate was washed and incubated with 100 µl per well of an HRP-conjugated goat anti-mouse IgG secondary antibody at a dilution of 1:10,000 for one hour at room temperature. Detection was performed using an Ultra TMB Substrate for 5 minutes at room temperature in the dark. The reaction was stopped with sulfuric acid and absorbances were read on a spectrophotometer at 450 nm.

  • Bovine Serum Albumin Antibody (<a href="/products/HA600086" style="font-weight: bold;text-decoration: underline;">HA600086</a>) in indirect ELISA.<br /><br />Indirect ELISA analysis of BSA was performed by coating wells of a 96-well plate with 100 µl per well of BSA standard diluted in carbonate/bicarbonate buffer, at a concentration of 1 µg/mL overnight at 4℃. Wells of the plate were washed, blocked with StartingBlock blocking buffer, and incubated with 100 µl per well of a mouse BSA monoclonal antibody starting at a concentration of 0.8 µg/mL for 2 hours at room temperature. The plate was washed and incubated with 100 µl per well of an HRP-conjugated goat anti-mouse IgG secondary antibody at a dilution of 1:10,000 for one hour at room temperature. Detection was performed using an Ultra TMB Substrate for 5 minutes at room temperature in the dark. The reaction was stopped with sulfuric acid and absorbances were read on a spectrophotometer at 450 nm.<br /><br />This antibody demonstrates high specificity for BSA and little or no crossreactivity to HSA (Human serum albumin), Goat serum and Rabbit serum.

    Bovine Serum Albumin Antibody (HA600086) in indirect ELISA.

    Indirect ELISA analysis of BSA was performed by coating wells of a 96-well plate with 100 µl per well of BSA standard diluted in carbonate/bicarbonate buffer, at a concentration of 1 µg/mL overnight at 4℃. Wells of the plate were washed, blocked with StartingBlock blocking buffer, and incubated with 100 µl per well of a mouse BSA monoclonal antibody starting at a concentration of 0.8 µg/mL for 2 hours at room temperature. The plate was washed and incubated with 100 µl per well of an HRP-conjugated goat anti-mouse IgG secondary antibody at a dilution of 1:10,000 for one hour at room temperature. Detection was performed using an Ultra TMB Substrate for 5 minutes at room temperature in the dark. The reaction was stopped with sulfuric acid and absorbances were read on a spectrophotometer at 450 nm.

    This antibody demonstrates high specificity for BSA and little or no crossreactivity to HSA (Human serum albumin), Goat serum and Rabbit serum.

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