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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.

Test your therapeutic antibodies in immunohistochemistry against a broad panel of normal frozen human tissue types in order to determine potential unintended binding. Our non-GLP TCR services are designed on the FDA recommendation outlined in their "Points to Consider in the Manufacture and Testing of Monoclonal Antibody Products for Human Use".

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CLCN1 / CLC‑1 Antibody (Biotin) LS‑C677553
CLC-1 antibody LS-C677553 is a biotin-conjugated rabbit polyclonal antibody to human CLC-1 (CLCN1). Validated for ELISA.
Antibody
Catalog
Size
Price
LS-C677553-50
50 µg
$285
LS-C677553-100
100 µg
$385

Popular CLCN1 / CLC-1 Products

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Product Description

CLCN1 / CLC-1 Antibody (Biotin) for ELISA LS-C677553

Specifications

Target
Human CLCN1 / CLC-1
Synonyms
CLCN1, Chloride channel protein 1, ClC-1, SMCC1, Chloride channel 1, CLC1
Host
Rabbit
Reactivity
Human (tested or 100% immunogen sequence identity)
Clonality
IgG Polyclonal
Conjugations
Biotin. Also available Unconjugated or conjugated with FITC, HRP.
Purification
Protein G purified
Modifications
Unmodified
Applications
  • ELISA
  • (applications tested for the base form of this product only)
Immunogen
CLCN1 / CLC-1 antibody was raised against recombinant human Chloride channel protein 1 protein (634-988AA)
Presentation
0.01 M PBS, pH 7.4, 0.03% ProClin™ 300, 50% Glycerol
Storage
Upon receipt, store at -20°C or -80°C. Avoid repeated freeze.
Restrictions
For research use only.
About CLCN1 / CLC-1
The CLCN family of voltage-dependent chloride channel genes comprises nine members (CLCN1-7, Ka and Kb) which demonstrate quite diverse functional characteristics while sharing significant sequence homology. The protein encoded by this gene regulates the electric excitability of the skeletal muscle membrane. Mutations in this gene cause two forms of inherited human muscle disorders: recessive generalized myotonia congenita (Becker) and dominant myotonia (Thomsen). P35523 NM_000083 NP_000074.2


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Requested From: United States
Date Requested: 10/23/2018

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