Rabbit SLC4A4/NBC Polyclonal Antibody | anti-SLC4A4/NBC antibody

SLC4A4/NBC Polyclonal Antibody

Cat. Num. AAA2566479

• Gene Names: SLC4A4; KNBC; NBC1; NBC2; pNBC; HNBC1; hhNMC; SLC4A5; NBCe1-A
• Reactivity: Human, Mouse, Rat
• Applications: Immunohistochemistry
• Purity: Affinity purification
• Synonyms: SLC4A4/NBC; Polyclonal Antibody; SLC4A4/NBC Polyclonal Antibody; SLC4A4; HNBC1; KNBC; NBC1; NBC2; NBCe1-A; SLC4A5; hhNMC; kNBC1; pNBC; anti-SLC4A4/NBC antibody

• Host: Rabbit
• Reactivity: Human, Mouse, Rat
• Clonality: Polyclonal
• Isotype: IgG
• Purity/Purification: Affinity purification
• Form/Format: PBS with 0.02% sodium azide, 50% glycerol, pH7.3
• Concentration: 1mg/mL (varies by lot)

• Applicable Applications for anti-SLC4A4/NBC antibody: Immunohistochemistry (IHC)
• Application Notes: IHC: 1:50-1:200
• Immunogen: Recombinant fusion protein of human SLC4A4 / NBC (NP_0037501)
• Conjugation: Unconjugated
• Preparation and Storage: Store at -20 degree C. Avoid freeze/thaw cycles.

Immunohistochemistry (IHC)

(Immunohistochemistry of paraffin-embedded Human prostate using SLC4A4 / NBC Polyclonal Antibody at dilution of 1:100 (40x lens).)

Immunohistochemistry (IHC)

(Immunohistochemistry of paraffin-embedded Mouse kidney using SLC4A4 / NBC Polyclonal Antibody at dilution of 1:100 (40x lens).)

Immunohistochemistry (IHC)

(Immunohistochemistry of paraffin-embedded Rat kidney using SLC4A4 / NBC Polyclonal Antibody at dilution of 1:100 (40x lens).)

Related Product Information for anti-SLC4A4/NBC antibody

This gene encodes a sodium bicarbonate cotransporter (NBC) involved in the regulation of bicarbonate secretion and absorption and intracellular pH. Mutations in this gene are associated with proximal renal tubular acidosis. Multiple transcript variants encoding different isoforms have been found for this gene.

Product Categories/Family for anti-SLC4A4/NBC antibody

Cancer; Metabolism; Neuroscience; Signal Transduction; Polyclonal Antibody

NCBI and Uniprot Product Information

• NCBI GI #: 148596928
• NCBI GeneID: 8671
• NCBI Accession #: NP_001091954.1
• NCBI GenBank Nucleotide #: NM_001098484.2
• UniProt Accession #: Q9Y6R1; O15153; Q8NEJ2; Q9H262; Q9NRZ1; Q9UIC0; Q9UIC1; Q9UP50; C4B714
• Molecular Weight: 123,181 Da
• NCBI Official Full Name: electrogenic sodium bicarbonate cotransporter 1 isoform 1
• NCBI Official Synonym Full Names: solute carrier family 4 (sodium bicarbonate cotransporter), member 4
• NCBI Official Symbol: SLC4A4
• NCBI Official Synonym Symbols: KNBC; NBC1; NBC2; pNBC; HNBC1; hhNMC; SLC4A5; NBCe1-A
• NCBI Protein Information: electrogenic sodium bicarbonate cotransporter 1; Na(+)/HCO3(-) cotransporter; kNBC1; sodium bicarbonate cotransporter 1 (sodium bicarbonate cotransporter, kidney; sodium bicarbonate cotransporter, pancreas); solute carrier family 4, sodium bicarbonate cot
• UniProt Protein Name: Electrogenic sodium bicarbonate cotransporter 1
• UniProt Gene Name: SLC4A4
• UniProt Synonym Gene Names: NBC; NBC1; NBCE1; Sodium bicarbonate cotransporter
• UniProt Entry Name: S4A4_HUMAN

NCBI Description

This gene encodes a sodium bicarbonate cotransporter (NBC) involved in the regulation of bicarbonate secretion and absorption and intracellular pH. Mutations in this gene are associated with proximal renal tubular acidosis. Multiple transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Oct 2008]

Uniprot Description

SLC4A4: 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. Defects in SLC4A4 are the cause of proximal renal tubular acidosis with ocular abnormalities (pRTA-OA); also known as renal tubular acidosis II. Caused by an impairment of bicarbonate absorption in the proximal tubule, proximal renal tubular acidosis (pRTA) is characterized by a decreased renal HCO3(-) threshold. pRTA-OA is an extremely rare autosomal recessive syndrome characterized by short stature, profound pRTA, mental retardation, bilateral glaucoma, cataracts and bandkeratopathy. Loss of interaction with and stimulation by CA4 is the cause of retinitis pigmentosa type 17 (RP17). Belongs to the anion exchanger (TC 2.A.31) family. 5 isoforms of the human protein are produced by alternative splicing.

Protein type: Transporter; Transporter, SLC family; Membrane protein, integral; Membrane protein, multi-pass

Chromosomal Location of Human Ortholog: 4q21

Cellular Component: basolateral plasma membrane; integral to plasma membrane; plasma membrane

Molecular Function: protein binding; inorganic anion exchanger activity; sodium:bicarbonate symporter activity

Biological Process: transport; bicarbonate transport; regulation of intracellular pH; ion transport; transmembrane transport

Disease: Renal Tubular Acidosis, Proximal, With Ocular Abnormalities And Mental Retardation