Rabbit Polyclonal SLC4A4/NBC antibody. Suitable for IHC-P, WB and reacts with Mouse, Rat, Human samples. Cited in 12 publications. Immunogen corresponding to Recombinant Fragment Protein within Human SLC4A4 aa 1-250.
pH: 7.3
Preservative: 0.05% Proclin 300
Constituents: 50% Glycerol (glycerin, glycerine), 49.95% PBS
IHC-P | WB | |
---|---|---|
Human | Tested | Tested |
Mouse | Tested | Expected |
Rat | Tested | Expected |
Species | Dilution info | Notes |
---|---|---|
Species Mouse | Dilution info 1/50.00000 - 1/200.00000 | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species Rat | Dilution info 1/50.00000 - 1/200.00000 | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species Human | Dilution info 1/50.00000 - 1/200.00000 | Notes Perform heat-mediated antigen retrieval with citrate buffer pH 6 before commencing with IHC staining protocol. |
Species | Dilution info | Notes |
---|---|---|
Species Human | Dilution info 1/500.00000 - 1/2000.00000 | Notes - |
Species | Dilution info | Notes |
---|---|---|
Species Mouse, Rat | Dilution info Use at an assay dependent concentration. | Notes - |
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Electrogenic sodium/bicarbonate cotransporter with a Na(+):HCO3(-) stoichiometry varying from 1:2 to 1:3. May regulate bicarbonate influx/efflux at the basolateral membrane of cells and regulate intracellular pH.
NBC, NBC1, NBCE1, SLC4A4, Electrogenic sodium bicarbonate cotransporter 1, Sodium bicarbonate cotransporter, Na(+)/HCO3(-) cotransporter, Solute carrier family 4 member 4, kNBC1
Rabbit Polyclonal SLC4A4/NBC antibody. Suitable for IHC-P, WB and reacts with Mouse, Rat, Human samples. Cited in 12 publications. Immunogen corresponding to Recombinant Fragment Protein within Human SLC4A4 aa 1-250.
pH: 7.3
Preservative: 0.05% Proclin 300
Constituents: 50% Glycerol (glycerin, glycerine), 49.95% PBS
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SLC4A4 also known as NBC (electrogenic Na+/bicarbonate cotransporter) is a protein that functions in the active transport of bicarbonate ions across cell membranes coupled with sodium ions. This cotransporter plays an essential role in maintaining the acid-base balance and cellular pH homeostasis. The SLC4A4 protein has a molecular mass of approximately 121 kDa. It expresses in various tissues with high levels found in the kidney and pancreas. Its activity is critical for efficient transport processes in epithelial cells contributing to the overall ion balance within these organs.
The activity of SLC4A4/NBC influences several physiological processes. This protein helps regulate bicarbonate reabsorption in renal proximal tubules which is fundamental for the body's buffering capacity. SLC4A4 can operate within complex systems involving other transport mechanisms to efficiently maintain proper ion concentrations and pH balance. It associates with proteins like carbonic anhydrase which facilitates the rapid interconversion of carbon dioxide and bicarbonate enhancing the efficiency of its transport function.
SLC4A4/NBC integrates into several key biological pathways that maintain bicarbonate and acid-base equilibrium. One such pathway is the renal tubular bicarbonate reclamation where it collaborates closely with proteins such as NHE3 (sodium hydrogen exchanger 3) to ensure sodium and bicarbonate absorption. Another pathway is the pancreatic bicarbonate secretion where its role complements secretor proteins to assimilate bicarbonates essential for neutralizing gastric acids.
SLC4A4/NBC correlates with significant clinical conditions affecting bicarbonate transport. Mutations or dysfunction in this transporter relate to proximal renal tubular acidosis a disorder characterized by impaired acid-base regulation in kidneys. Additionally it associates with migraine disorders where alterations in pH and ion flow might play a role. Through these conditions SLC4A4 may connect with other bicarbonate transporters such as SLC4A7 to provide insights into pathophysiological mechanisms involving ionic imbalances.
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Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of rat lung tissue labelling SLC4A4/NBC with ab187511 at 1/200. Magnification: 400x.
All lanes: Western blot - Anti-SLC4A4/NBC antibody (ab187511) at 1/500 dilution
Lane 1: PC3 cell extract
Lane 2: A549 cell extract
Developed using the ECL technique.
Predicted band size: 121 kDa
Immunohistochemical analysis of paraffin embedded mouse kidney tissue labeling SLC4A4/NBC with ab187511 at 1:100 dilution.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human lung cancer tissue labelling SLC4A4/NBC with ab187511 at 1/200. Magnification: 400x.
Immunohistochemistry (Formalin/PFA-fixed paraffin-embedded sections) analysis of human liver cancer tissue labelling SLC4A4/NBC with ab187511 at 1/200. Magnification: 400x.
Immunohistochemical analysis of paraffin embedded rat kidney tissue labeling SLC4A4/NBC with ab187511 at 1:100 dilution.
Image collected and cropped by CiteAb under a CC-BY license from the publication
SLC4A4/NBC western blot using anti-SLC4A4/NBC antibody ab187511. Publication image and figure legend from Hwang, S., Shin, D. M., et al., 2019, Molecules, PubMed 31546841.
ab187511 was used in this publication in western blot. This may not be the same as the application(s) guaranteed by Abcam. For a full list of applications guaranteed by Abcam for ab187511 please see the product overview.
Surface protein expression of AE2 protein was decreased by DSF treatment. (A) Analysis of AE2 mRNA expression at rising concentrations from 0.1–4 μM DSF for 48 h (n = 5). (B) Protein expression of AE2 at indicated DSF concentration. (C) Analysis of relative AE2 intensity (n = 3, * p < 0.05, *** p < 0.001). (D) Immunostained images of AE2 (red), nucleus (DAPI, blue) and merge of cell morphology (TPM-T, gray) with and without DSF treatment. The scale bars represent 20 μm. (E) The surface expression of AE2 after treatment with 2 μM DSF. The β-actin and input AE2 blots were used as loading controls. (F) Analysis of relative intensity of AE2 for input and biotinylated (Bio) blot. Bars represent mean ± SEM (n = 3, ** p < 0.01). (G) Protein expressions of NBCe1 and NBCn1. (H) Analysis of relative intensity of NBCe1 and NBCn1 blots. Bars represent mean ± SEM. (I) Protein expressions of LC3B and p62. The β-actin blot was used as a loading control. (J) Analysis of relative intensity of LC3B and p62 blots. Bars represent mean ± SEM.
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