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Work with LifeSpan to design a custom immunohistochemistry to address your specific biological question. Outsource the entire localization process without having to worry about finding and characterizing target specific antibodies, sourcing and validating difficult-to-find tissues, and having the ability to interpret the resulting immunostaining in relation to complex human pathologies.

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ALB / Serum Albumin Antibody LS‑C60068
Serum Albumin antibody LS-C60068 is an unconjugated rabbit polyclonal antibody to mouse Serum Albumin (ALB). Validated for ELISA and WB.
Catalog
Size
Price
LS-C60068-1000
1000 µg
Unavailable

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Product Description

Serum Albumin antibody LS-C60068 is an unconjugated rabbit polyclonal antibody to mouse Serum Albumin (ALB). Validated for ELISA and WB.
About ALB / Serum Albumin
Albumin ALB) is a soluble, monomeric protein which comprises about one-half of the blood serum protein. Albumin functions primarily as a carrier protein for steroids, fatty acids, and thyroid hormones and plays a role in stabilizing extracellular fluid volume. Mutations in the ALB gene on chromosome 4 result in various anomalous proteins. Albumin is a globular unglycosylated serum protein of molecular weight 65000. P02768 NM_000477 NP_000468.1

ALB Antibody, Albumin (32 AA) Antibody, Albumin (AA 34) Antibody, Albumin Antibody, Growth-inhibiting protein 20 Antibody, PRO1341 Antibody, PRO0883 Antibody, Serum albumin Antibody, PRO0903 Antibody


Specifications

Target
Mouse ALB / Serum Albumin
Host
Rabbit
Reactivity
Mouse (tested or 100% immunogen sequence identity)
Clonality
Polyclonal
Conjugations
Unconjugated
Purification
Immunoaffinity purified
Modifications
Unmodified
Applications
  • Western blot
  • ELISA (1:10000 - 1:50000)
Immunogen
Mouse Serum Albumin.
Specificity
anti-Rabbit Serum. Analysis by SDS-PAGE was used to determine that this preparation is substantially free of aggregates and shows a banding pattern consistent with purified Rabbit IgG
Usage
Suitable for most immunological methods. This product has been assayed against 1.0 ug of Mouse Serum Albumin in a standard sandwich ELISA using Peroxidase conjugated Affinity Purified Donkey anti-Rabbit IgG [H&L] MX catalog no. LS-C60943 and TMB as a substrate for 30 minutes at room temperature.
Presentation
0.02 M potassium phosphate, 0.15 M sodium chloride, pH 7.2, 0.01% sodium azide.
Storage
Short term: -20°C; Long term: -20°C.
Restrictions
For research use only.
Guarantee
This antibody carries the LSBio 100% Guarantee.

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Images


Western blot

Anti-MSA Antibody - Western Blot. Western Blot showing detection of mouse serum albumin (0.1 ug) in lane 2. MW markers are in lane 1. Protein was run on a 4-20% gel, then transferred to 0.45 micron nitrocellulose. After blocking with 1% BSA-TTBS (MB-013, diluted to 1X) 30 min at 20°C, primary antibody was used at 1:1000 overnight at 4°C. Anti-Rabbit IgG (H&L) (GOAT) antibody IRDye800CW (p/n secondary antibody was used at 1:20000 in Blocking Buffer for Fluorescent Western Blot (p/n MB-070) and imaged on the LiCor Odyssey imaging system. Arrow indicates correct 69 kD molecular weight position expected for mouse serum albumin.
Anti-MSA Antibody - Western Blot. Western Blot showing detection of mouse serum albumin (0.1 ug) in lane 2. MW markers are in lane 1. Protein was run on a 4-20% gel, then transferred to 0.45 micron nitrocellulose. After blocking with 1% BSA-TTBS (MB-013, diluted to 1X) 30 min at 20°C, primary antibody was used at 1:1000 overnight at 4°C. Anti-Rabbit IgG (H&L) (GOAT) antibody IRDye800CW (p/n secondary antibody was used at 1:20000 in Blocking Buffer for Fluorescent Western Blot (p/n MB-070) and imaged on the LiCor Odyssey imaging system. Arrow indicates correct 69 kD molecular weight position expected for mouse serum albumin.

Western blot

Rb-a-Mouse Serum Albumin - SDS-PAGE. Coomassie stained SDS-PAGE of 1.0 ug of Rb-a-Mouse Serum Albumin separated in a 4-20% gradient gel under reducing conditions (lane 1) and non-reducing conditions (lane 3). Molecular weight standards are shown in lane 2. Analysis by SDS-PAGE shows a banding pattern consistent with purified Rabbit IgG.
Rb-a-Mouse Serum Albumin - SDS-PAGE. Coomassie stained SDS-PAGE of 1.0 ug of Rb-a-Mouse Serum Albumin separated in a 4-20% gradient gel under reducing conditions (lane 1) and non-reducing conditions (lane 3). Molecular weight standards are shown in lane 2. Analysis by SDS-PAGE shows a banding pattern consistent with purified Rabbit IgG.

Western blot

Anti-MSA Antibody - Western Blot. Western Blot showing detection of mouse serum albumin (0.1 ug) in lane 2. MW markers are in lane 1. Protein was run on a 4-20% gel, then transferred to 0.45 micron nitrocellulose. After blocking with 1% BSA-TTBS (MB-013, diluted to 1X) 30 min at 20°C, primary antibody was used at 1:1000 overnight at 4°C. Anti-Rabbit IgG (H&L) (GOAT) antibody IRDye800CW (p/n secondary antibody was used at 1:20000 in Blocking Buffer for Fluorescent Western Blot (p/n MB-070) and imaged on the LiCor Odyssey imaging system. Arrow indicates correct 69 kD molecular weight position expected for mouse serum albumin.
Anti-MSA Antibody - Western Blot. Western Blot showing detection of mouse serum albumin (0.1 ug) in lane 2. MW markers are in lane 1. Protein was run on a 4-20% gel, then transferred to 0.45 micron nitrocellulose. After blocking with 1% BSA-TTBS (MB-013, diluted to 1X) 30 min at 20°C, primary antibody was used at 1:1000 overnight at 4°C. Anti-Rabbit IgG (H&L) (GOAT) antibody IRDye800CW (p/n secondary antibody was used at 1:20000 in Blocking Buffer for Fluorescent Western Blot (p/n MB-070) and imaged on the LiCor Odyssey imaging system. Arrow indicates correct 69 kD molecular weight position expected for mouse serum albumin.

Western blot

Rb-a-Mouse Serum Albumin - SDS-PAGE. Coomassie stained SDS-PAGE of 1.0 ug of Rb-a-Mouse Serum Albumin separated in a 4-20% gradient gel under reducing conditions (lane 1) and non-reducing conditions (lane 3). Molecular weight standards are shown in lane 2. Analysis by SDS-PAGE shows a banding pattern consistent with purified Rabbit IgG.
Rb-a-Mouse Serum Albumin - SDS-PAGE. Coomassie stained SDS-PAGE of 1.0 ug of Rb-a-Mouse Serum Albumin separated in a 4-20% gradient gel under reducing conditions (lane 1) and non-reducing conditions (lane 3). Molecular weight standards are shown in lane 2. Analysis by SDS-PAGE shows a banding pattern consistent with purified Rabbit IgG.

Western blot

Anti-MSA Antibody - Western Blot. Western Blot showing detection of mouse serum albumin (0.1 ug) in lane 2. MW markers are in lane 1. Protein was run on a 4-20% gel, then transferred to 0.45 micron nitrocellulose. After blocking with 1% BSA-TTBS (MB-013, diluted to 1X) 30 min at 20°C, primary antibody was used at 1:1000 overnight at 4°C. Anti-Rabbit IgG (H&L) (GOAT) antibody IRDye800CW (p/n secondary antibody was used at 1:20000 in Blocking Buffer for Fluorescent Western Blot (p/n MB-070) and imaged on the LiCor Odyssey imaging system. Arrow indicates correct 69 kD molecular weight position expected for mouse serum albumin.
Anti-MSA Antibody - Western Blot. Western Blot showing detection of mouse serum albumin (0.1 ug) in lane 2. MW markers are in lane 1. Protein was run on a 4-20% gel, then transferred to 0.45 micron nitrocellulose. After blocking with 1% BSA-TTBS (MB-013, diluted to 1X) 30 min at 20°C, primary antibody was used at 1:1000 overnight at 4°C. Anti-Rabbit IgG (H&L) (GOAT) antibody IRDye800CW (p/n secondary antibody was used at 1:20000 in Blocking Buffer for Fluorescent Western Blot (p/n MB-070) and imaged on the LiCor Odyssey imaging system. Arrow indicates correct 69 kD molecular weight position expected for mouse serum albumin.

Western blot

Rb-a-Mouse Serum Albumin - SDS-PAGE. Coomassie stained SDS-PAGE of 1.0 ug of Rb-a-Mouse Serum Albumin separated in a 4-20% gradient gel under reducing conditions (lane 1) and non-reducing conditions (lane 3). Molecular weight standards are shown in lane 2. Analysis by SDS-PAGE shows a banding pattern consistent with purified Rabbit IgG.
Rb-a-Mouse Serum Albumin - SDS-PAGE. Coomassie stained SDS-PAGE of 1.0 ug of Rb-a-Mouse Serum Albumin separated in a 4-20% gradient gel under reducing conditions (lane 1) and non-reducing conditions (lane 3). Molecular weight standards are shown in lane 2. Analysis by SDS-PAGE shows a banding pattern consistent with purified Rabbit IgG.

Western blot

Anti-MSA Antibody - Western Blot. Western Blot showing detection of mouse serum albumin (0.1 ug) in lane 2. MW markers are in lane 1. Protein was run on a 4-20% gel, then transferred to 0.45 micron nitrocellulose. After blocking with 1% BSA-TTBS (MB-013, diluted to 1X) 30 min at 20°C, primary antibody was used at 1:1000 overnight at 4°C. Anti-Rabbit IgG (H&L) (GOAT) antibody IRDye800CW (p/n secondary antibody was used at 1:20000 in Blocking Buffer for Fluorescent Western Blot (p/n MB-070) and imaged on the LiCor Odyssey imaging system. Arrow indicates correct 69 kD molecular weight position expected for mouse serum albumin.
Anti-MSA Antibody - Western Blot. Western Blot showing detection of mouse serum albumin (0.1 ug) in lane 2. MW markers are in lane 1. Protein was run on a 4-20% gel, then transferred to 0.45 micron nitrocellulose. After blocking with 1% BSA-TTBS (MB-013, diluted to 1X) 30 min at 20°C, primary antibody was used at 1:1000 overnight at 4°C. Anti-Rabbit IgG (H&L) (GOAT) antibody IRDye800CW (p/n secondary antibody was used at 1:20000 in Blocking Buffer for Fluorescent Western Blot (p/n MB-070) and imaged on the LiCor Odyssey imaging system. Arrow indicates correct 69 kD molecular weight position expected for mouse serum albumin.

Western blot

Rb-a-Mouse Serum Albumin - SDS-PAGE. Coomassie stained SDS-PAGE of 1.0 ug of Rb-a-Mouse Serum Albumin separated in a 4-20% gradient gel under reducing conditions (lane 1) and non-reducing conditions (lane 3). Molecular weight standards are shown in lane 2. Analysis by SDS-PAGE shows a banding pattern consistent with purified Rabbit IgG.
Rb-a-Mouse Serum Albumin - SDS-PAGE. Coomassie stained SDS-PAGE of 1.0 ug of Rb-a-Mouse Serum Albumin separated in a 4-20% gradient gel under reducing conditions (lane 1) and non-reducing conditions (lane 3). Molecular weight standards are shown in lane 2. Analysis by SDS-PAGE shows a banding pattern consistent with purified Rabbit IgG.


Requested From: 
Date Requested: 6/19/2018

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