ALMS1 Antibody

Novus Biologicals, part of Bio-Techne | Catalog # NBP3-06330

Novus Biologicals, part of Bio-Techne
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NBP3-06330-100ul
NBP3-06330-50ul
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Key Product Details

Species Reactivity

Validated:

Human

Applications

Immunohistochemistry-Paraffin

Label

Unconjugated

Antibody Source

Polyclonal Rabbit IgG

Concentration

Please see the vial label for concentration. If unlisted please contact technical services.

View all ALMS1 Antibodies »

Product Summary for ALMS1 Antibody

Immunogen

Produced in rabbits immunized with E. coli-derived Human ALMS1 fragment.

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Description

This antibody can be stored at 2C-8C for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20C to -80C. Avoid repeated freeze-thaw cycles.

Scientific Data Images for ALMS1 Antibody

Immunohistochemistry-Paraffin: ALMS1 Antibody [NBP3-06330]

Immunohistochemistry-Paraffin: ALMS1 Antibody [NBP3-06330]

Immunohistochemistry-Paraffin: ALMS1 Antibody [NBP3-06330] - Immunochemical staining of human ALMS1 in human rectum with rabbit polyclonal antibody at 1:100 dilution, formalin-fixed paraffin embedded sections.

Applications for ALMS1 Antibody

Application
Recommended Usage

Immunohistochemistry-Paraffin

1:50-1:200
Please Note: Optimal dilutions of this antibody should be experimentally determined.

Formulation, Preparation, and Storage

Purification

Antigen and protein A Affinity-purified

Formulation

PBS

Preservative

0.03% Proclin 300

Concentration

Please see the vial label for concentration. If unlisted please contact technical services.

Shipping

The product is shipped with polar packs. Upon receipt, store it immediately at the temperature recommended below.

Stability & Storage

Store at 4C short term. Aliquot and store at -20C long term. Avoid freeze-thaw cycles.

Background: ALMS1

Mutations in the ALMS1 gene are the cause of Alstrom syndrome, a rare autosomal recessive disease characterized by type 2 diabetes mellitus, obesity, cardiomyopathy, and neurosensory defects such as cone-rod retinal dystrophy, and hearing loss. In the cell, ALMS1 localizes to basal bodies of ciliated cells and centrosomes and is thus a member of proteins associated with genetic ciliopathies. ALMS1 is also known as KIAA0328 and ALSS.

Alternate Names

Alstrom syndrome 1, Alstrom syndrome protein 1, DKFZp686A118, DKFZp686D1828, KIAA0328ALSS

Gene Symbol

ALMS1

Additional ALMS1 Products

Product Documents for ALMS1 Antibody

Product Datasheets

Certificate of Analysis

To download a Certificate of Analysis, please enter a lot number in the search box below.

Product Specific Notices for ALMS1 Antibody

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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