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Mouse Anti-CA4 Recombinant Antibody (CBYY-C0002) (CBMAB-C0007-YY)

This product is mouse antibody that recognizes CA4. The antibody CBYY-C0002 can be used for immunoassay techniques such as: IHC, IP, WB
See all CA4 antibodies

Summary

Host Animal
Mouse
Specificity
Human, Rat
Clone
CBYY-C0002
Antibody Isotype
IgG2b, κ
Application
IH, WB, IF, IP

Basic Information

Immunogen
Recombinant CA4 (Ala19~Lys283) expressed in E.coli.
Host Species
Mouse
Specificity
Human, Rat
Antibody Isotype
IgG2b, κ
Clonality
Monoclonal
Application Notes
The COA includes recommended starting dilutions, optimal dilutions should be determined by the end user.
ApplicationNote
WB0.5-2 µg/ml
IHC5-20 µg/ml
IF(ICC)5-20 µg/ml

Formulations & Storage [For reference only, actual COA shall prevail!]

Format
Liquid
Buffer
0.5 mg/mL
Preservative
PBS, 5% trehalose
Concentration
1 mg/ml
Storage
Store at +4°C short term (1-2 weeks). Aliquot and store at -20°C long term. Avoid repeated freeze/thaw cycles.

Target

Full Name
Carbonic Anhydrase 4
Entrez Gene ID
UniProt ID
Alternative Names
Colony Stimulating Factor 1 Receptor; McDonough Feline Sarcoma Viral (V-Fms) Oncogene Homolog; Proto-Oncogene C-Fms; CSF-1 Receptor; CD115 Antigen; EC 2.7.10.1; M-CSF-R; CSF-1R; FMS; Macrophage Colony Stimulating Factor I Receptor;
Function
Reversible hydration of carbon dioxide. May stimulate the sodium/bicarbonate transporter activity of SLC4A4 that acts in pH homeostasis. It is essential for acid overload removal from the retina and retina epithelium, and acid release in the choriocapillaris in the choroid.
Biological Process
Bicarbonate transport Source: DFLAT
One-carbon metabolic process Source: GO_Central
Cellular Location
Cell membrane
Involvement in disease
Retinitis pigmentosa 17 (RP17): The disease is caused by variants affecting the gene represented in this entry. Defective acid overload removal from retina and retinal epithelium, due to mutant CA4, is responsible for photoreceptor degeneration, indicating that impaired pH homeostasis is the most likely cause underlying the RP17 phenotype. A retinal dystrophy belonging to the group of pigmentary retinopathies. Retinitis pigmentosa is characterized by retinal pigment deposits visible on fundus examination and primary loss of rod photoreceptor cells followed by secondary loss of cone photoreceptors. Patients typically have night vision blindness and loss of midperipheral visual field. As their condition progresses, they lose their far peripheral visual field and eventually central vision as well.
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For research use only. Not intended for any clinical use.

Custom Antibody Labeling

We also offer labeled antibodies developed using our catalog antibody products and nonfluorescent conjugates (HRP, AP, Biotin, etc.) or fluorescent conjugates (Alexa Fluor, FITC, TRITC, Rhodamine, Texas Red, R-PE, APC, Qdot Probes, Pacific Dyes, etc.).

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