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Anti-Carbonic Anhydrase 2 / CA2 Antibody (A283276)

$435

Sheep polyclonal antibody to Carbonic Anhydrase 2 / CA2 for WB, IF and Immunodiffusion.

Shipping Information

$40
Dispatched from St. Louis, MO.
Lead Time: 5-7 business days.
Name
Anti-Carbonic Anhydrase 2 / CA2 Antibody
Description
Sheep polyclonal antibody to Carbonic Anhydrase 2 / CA2.
Specificity
This antibody recognises human carbonic anhydrase II, also known as Carbonate dehydratase II or Carbonic anhydrase C. Carbonic anhydrase II is a 259 amino acid ~30 kDa enzyme essential for bone resorption and osteoclast differrentiation.Mutations in the CA2 gene has been identified as the cause of osteopetrosis, autosomal recessive 3 (OPTB3), a rare disease characterized by particularly dense bone, cerebral calcification and renal tubular acidosis (Shah et al 2004).Product identity is confirmed by double diffusion vs human CAII. No reactivity is seen in immunodiffusion against CAI.
Applications
WB, IF, Immunodiffusion
Dilutions
WB: 1:1,000
Reactivity
Human
Immunogen
Purified human carbonic anhydrase II (CAII) prepared from erythrocytes.
Host
Sheep
Clonality
Polyclonal
Isotype
IgG
Conjugate

Unconjugated

Concentration
Lot Specific
Molecular Weight
Approximately 18 kDa in rat adrenomedullary chromaffin cell lysates.
Product Form
Liquid
Formulation
Supplied in Glycine Buffered Saline with <0.1% Sodium Azide, 0.1% EACA, 0.01% Benzamidine, and 1 mM EDTA.
Storage
Shipped at ambient temperature. Upon delivery aliquot and store at -20°C. When thawed, aliquot the sample as needed. Short term (up to 4 weeks): store at 4°C. Long term: store at -20°C. Avoid freeze / thaw cycles. Storage in frost free freezers is not recommended.
General Notes
Sheep anti Human carbonic anhydrase II antibody recognizes human carbonic anhydrase II, also known as Carbonate dehydratase II or Carbonic anhydrase C. Carbonic anhydrase II is a 259 amino acid ~30 kDa enzyme essential for bone resorption and osteoclast differrentiation.Mutations in the CA2 gene has been identified as the cause of osteopetrosis, autosomal recessive 3 (OPTB3), a rare disease characterized by particularly dense bone, cerebral calcification and renal tubular acidosis (Shah et al 2004).Product identity is confirmed by double diffusion vs human CAII. No reactivity is seen in immunodiffusion against CAI.
Disclaimer
This product is for research use only. It is not intended for diagnostic or therapeutic use.
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