CLCN7 Antibody - BSA Free

Novus Biologicals | Catalog # NBP3-29958

Novus Biologicals
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Key Product Details

Species Reactivity

Human

Applications

Immunoprecipitation

Label

Unconjugated

Antibody Source

Polyclonal Rabbit IgG

Format

BSA Free
View all CLCN7 Primary Antibodies »

Product Specifications

Immunogen

Between 50 and 100

Clonality

Polyclonal

Host

Rabbit

Isotype

IgG

Scientific Data Images for CLCN7 Antibody - BSA Free

CLCN7 Antibody

Immunoprecipitation:CLCN7 AntibodyNBP3-29958] -

Immunoprecipitation:CLCN7 AntibodyNBP3-29958] -Detection of human CLCN7 by western blot of immunoprecipitates. Samples: Whole cell lysate (0.5 or 1.0 mg per IP reaction; 20% of IP loaded) from Jurkat cells prepared using NETN lysis buffer. Antibodies: Affinity purified rabbit anti-CLCN7 antibody NBP3-29958 (lot NBP3-29958-1) used for IP at 6 µg per reaction. CLCN7 was also immunoprecipitated by rabbit anti-CLCN7 antibody. For blotting immunoprecipitated CLCN7, NBP3-29958 was used at 0.4 µg/ml. Detection: Chemiluminescence with an exposure time of 3 minutes.

Applications for CLCN7 Antibody - BSA Free

Application
Recommended Usage

Immunoprecipitation

Optimal dilutions of this antibody should be experimentally determined.

Formulation, Preparation, and Storage

Purification

Affinity purified

Formulation

Tris-citrate/phosphate pH 7 -8.

Format

BSA Free

Preservative

0.09% Sodium Azide

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. Do not freeze.

Background: CLCN7

The product of this gene belongs to the CLC chloride channel family of proteins. Chloride channels play important roles in the plasma membrane and in intracellular organelles. This gene encodes chloride channel 7. Defects in this gene are the cause of osteopetrosis autosomal recessive type 4 (OPTB4), also called infantile malignant osteopetrosis type 2 as well as the cause of autosomal dominant osteopetrosis type 2 (OPTA2), also called autosomal dominant Albers-Schonberg disease or marble disease autosoml dominant. Osteopetrosis is a rare genetic disease characterized by abnormally dense bone, due to defective resorption of immature bone. OPTA2 is the most common form of osteopetrosis, occurring in adolescence or adulthood.

Alternate Names

chloride channel 7, Chloride channel protein 7, CLC-7, CLC7FLJ39644, FLJ26686, H(+)/Cl(-) exchange transporter 7, OPTA2FLJ46423, OPTB4

Gene Symbol

CLCN7

Additional CLCN7 Products

Product Documents for CLCN7 Antibody - BSA Free

Certificate of Analysis

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Product Specific Notices for CLCN7 Antibody - BSA Free

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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Protocols

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FAQs

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