Recombinant Anti-Carbonic Anhydrase VB Antibody, Rabbit Monoclonal sinobiological 12285-R008

$171.00
In stock
SKU
12285-R008
Catalog No.SizePrice (USD)
12285-R008-5050 µL$177.58
12285-R008-100100 µL$340.51

General Information

Product nameRecombinant Anti-Carbonic Anhydrase VB Antibody, Rabbit Monoclonal
Validated applicationsIHC-P (FAQ Protocol)
Species reactivityReacts with: Human
SpecificityHuman Carbonic Anhydrase VB Has cross-reactivity in ELISA with Human CA2 Human CA3 Human CA5A No cross-reactivity in ELISA with Human CA8 Human CA4
ImmunogenRecombinant Human Carbonic Anhydrase VB / CA5B protein (Catalog#12285-H08E)
PreparationThis antibody was obtained from a rabbit immunized with purified, recombinant Human Carbonic Anhydrase VB / CA5B (rh Carbonic Anhydrase VB / CA5B; Catalog#12285-H08E; Q9Y2D0; Cys34-Pro317).
SourceMonoclonal Rabbit IgG Clone #008
PurificationProtein A
Formulation0.2 μm filtered solution in PBS
ConjugateUnconjugated
FormLiquid
ShippingThis antibody is shipped as liquid solution at ambient temperature. Upon receipt, store it immediately at the temperature recommended below.
StorageThis antibody can be stored at 2℃-8℃ for one month without detectable loss of activity. Antibody products are stable for twelve months from date of receipt when stored at -20℃ to -80℃. Preservative-Free. Avoid repeated freeze-thaw cycles.

Synonyms: Anti-CA-VB Antibody; Anti-CAVB Antibody

Image / Experimental Information

Image 1 DescriptionImmunochemical staining of human CA5B in human placenta with rabbit monoclonal antibody (1:100, formalin-fixed paraffin embedded sections).
Image 1 Alt TextHuman Carbonic Anhydrase VB Immunohistochemistry(IHC) 4620
Image 1 URLSource image
Image 2 DescriptionImmunochemical staining of human CA5B in human placenta with rabbit monoclonal antibody (1:100, formalin-fixed paraffin embedded sections).
Image 2 Alt TextHuman EGFR/HER1 Immunohistochemistry(IHC) 4621
Image 2 URLSource image
Image 3 DescriptionImmunochemical staining of human CA5B in human placenta with rabbit monoclonal antibody (1:100, formalin-fixed paraffin embedded sections).
Image 3 Alt TextHuman EGFR/HER1 Immunohistochemistry(IHC) 4622
Image 3 URLSource image

Background Information

Full Namecarbonic anhydrase VB, mitochondrial
DescriptionCarbonic anhydrase 5B, also known as carbonate dehydratase VB, carbonic anhydrase VB, CA-VB and CA5B, is amember of the alpha-carbonic anhydrase family. The strongest expression of CA5B / CA-VB is in heart, pancreas, kidney, placenta, lung, and skeletal muscle. It is not expressed in liver. Carbonic anhydrases (CAs) are a large family of zinc metalloenzymes first discovered in 1933 that catalyze the reversible hydration of carbon dioxide. CAs participate in a variety of biological processes, including respiration, calcification, acid-base balance, bone resorption, and the formation of aqueous humor, cerebrospinal fluid, saliva, and gastric acid. CAs show extensive diversity in tissue distribution and in their subcellular localization. CA5B / CA-VB is localized in the mitochondria and shows the highest sequence similarity to the other mitochondrial CA5A / CA-VA. CA5B / CA-VB has a wider tissue distribution than CA5A / CA-VA, which is restricted to the liver. The differences in tissue distribution suggest that the two mitochondrial carbonic anhydrases evolved to assume different physiologic roles. CA5A / CA-VA is activated by histamine, L-adrenaline, L- and D-histidine, and L- and D-phenylalanine. It is inhibited by coumarins, sulfonamide derivatives such as acetazolamide and Foscarnet (phosphonoformate trisodium salt). CA5B / CA-VB is inhibited by coumarins, sulfonamide derivatives such as acetazolamide (AZA), saccharin and Foscarnet (phosphonoformate trisodium salt).
References
  1. Fujikawa-Adachi K, et al.,1999, J Biol Chem. 274 (30): 21228-33.
  2. Liao, S.Y. et al., 2003, J. Med. Genet. 40:257 - 262.
  3. Temperini C.et al., 2006, Chemistry 12: 7057-66.
  4. Temperini C.et al., 2006, J. Med. Chem. 49: 3019-27.
  5. Supuran, C. T. et al., 2008, Curr Pharm Des. 14 (7): 601-602.
  6. Elleuche, S. et al., 2009, Curr Genet. 55 (2): 211-222.
  7. Maresca, A.et al., 2009, J. Am. Chem. Soc. 131:3057-3062.

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