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CLCN7, Rabbit, Monoclonal Antibody, Abnova™

Rabbit monoclonal antibody raised against a human CLCN7 peptide using ARM Technology.

Supplier:  Abnova Corporation H00001186K

Catalog No. 89-205-558


Includes: Up to three rabbit IgG clones of 1mg each will be delivered to customer.

Description

Description

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. [provided by RefSeq

Library Construction: Nonfusion antibody library from rabbit spleen (ARM Technology)
Expression: Overexpression vector and transfection into 293H cell line

Order Info

  1. Customer may provide cell or tissue lysate for antibody screening.
  2. Rabbit monoclonal antibody generated by ARM technology is amenable to antibody engineering including F(ab)2, IgG, scFv and different Fc and non-Fc conjugates per customer request.

Specifications

Specifications

CLCN7
Monoclonal
Unconjugated
In 1X PBS, pH 7.4
CLCN7
CLCN7
A synthetic peptide of human CLCN7
RUO
1186
Store at -20°C or lower. Aliquot to avoid repeated freezing and thawing.
IgG
ELISA, Western Blot
1mg
chloride channel 7
CLCN7
CLC-7, CLC7, FLJ26686, FLJ39644, FLJ46423, OPTA2, OPTB4
Rabbit
1 mg x up to 3 Abs
Primary
Human
Liquid
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