Merck Millipore代理AB2281 Anti-Na+K+Cl- Cotransporter 2 Antibody;store at +2℃ to +8℃

2025-06-28

货号:AB2281

品牌:Merck Millipore

规格:100Ug

目录价:¥4967.00

市场价格:¥4221.95

会员价格:¥3973.60

金山科研平台,产品价格货期咨询微信:jinshanbio Description: Anti-Na+K+Cl- Cotransporter 2 Antibody | AB2281 View All» Promotional Text: Special Shipping Offer on Antibodies100% Performance Guaranteed View All» Specificity: This antibody recognizes the cytoplasmic domain of NA+K+CL- Cotransporter 2. View All» Molecular Weight: ~150 kDa View All» Epitope: Cytoplasmic domain View All» Immunogen: KLH conjugate followed by NA+K+CL- Cotransporter 2 corresponding to the cytoplasmic domain. View All» Background Information: The sodium-potassium-chloride cotransporter isoform 2 is kidney-specific and is found on the apical membrane of the thick ascending limb of Henle's loop and the macula densa. It accounts for most of the NaCl resorption with the stoichiometry of 1Na:1K:2Cl and is sensitive to such diuretics as furosemide and bumetanide. Some Bartter-like syndromes result from defects in this gene. SLC12A1 is kidney specific and is essential in the regulation of ionic balance and cell volume. It is a component of an electrically silent transporter system, mediating sodium and chloride reabsorption. Defects in SLC12A1 are the cause of Bartter syndrome type 1, an autosomal recessive disorder characterized by impaired salt reabsorption in the thick ascending loop of Henle with pronounced salt wasting, hypokalemic metabolic alkalosis, and varying degrees of hypercalciuria. View All» Species Reactivity:

  • Rat

  • Mouse

  • Human

    View All» Species Reactivity Note: Proven to react with human, rat and mouse. View All» Control: Rat liver lysates View All» Quality Assurance: Western Blot Analysis: 1:2,000 dilution of this lot detected NA+K+CL- Cotransporter 2 on 10 µg of rat liver lysate. View All» Purification Method: Antigen affinity purified View All» Presentation: Purified rabbit polyclonal antibody in buffer containing 0.1M Tris-Glycine (pH7.4) 150mM NaCl with 0.05% NaN3. View All» Storage Conditions: Stable for 1 year at 2-8ºC from date of receipt. View All» UniProt Number: Q13621 View All» Entrez Gene Number: NM_000338.2 View All» Gene Symbol:
    • SLC12A1

    • BSC1

    • MGC48843

    • NKCC2

      View All» Alternate Names:
      • Bumetanide-sensitive sodium-(potassium)-chloridecotransporter 2

      • Kidney-specific Na-K-Cl symporter

      • NKCC2A variant A

      • Na-K-2Cl cotransporter

      • sodium potassium chloride cotransporter 2

      • solute carrier family 12 (sodium/potassium/chloridetransporters), member 1

        View All» Usage Statement: Unless otherwise stated in our catalog or other company documentation accompanying the product(s), our products are intended for research use only and are not to be used for any other purpose, which includes but is not limited to, unauthorized commercial uses, in vitro diagnostic uses, ex vivo or in vivo therapeutic uses or any type of consumption or application to humans or animals. View All» Key Applications: Western Blotting View All» Entrez Gene Summary: The sodium-potassium-chloride cotransporter isoform 2 is kidney-specific and is found on the apical membrane of the thick ascending limb of Henle's loop and the macula densa. It accounts for most of the NaCl resorption with the stoichiometry of 1Na:1K:2Cl and is sensitive to such diuretics as furosemide and bumetanide. Some Bartter-like syndromes result from defects in this gene. [provided by RefSeq]. View All» UniProt Summary: FUNCTION: Electrically silent transporter system. Mediates sodium and chloride reabsorption. Plays a vital role in the regulation of ionic balance and cell volume.SUBCELLULAR LOCATION: Membrane; Multi-pass membrane protein. TISSUE SPECIFICITY:Kidney specific.DISEASE: Defects in SLC12A1 are the cause of Bartter syndrome type 1 (BS1) [MIM:601678]. BS refers to a group of autosomal recessive disorders characterized by impaired salt reabsorption in the thick ascending loop of Henle with pronounced salt wasting, hypokalemic metabolic alkalosis, and varying degrees of hypercalciuria. BS1 is a life-threatening condition beginning in utero, with marked fetal polyuria that leads to polyhydramnios and premature delivery. Another hallmark of BS1 is a marked hypercalciuria and, as a secondary consequence, the development of nephrocalcinosis and osteopenia. Ref.1SIMILARITIY: Belongs to the SLC12A transporter family. View All» Product Name: Anti-Na+K+Cl- Cotransporter 2 View All» Concentration: 1 mg/mL View All» Antibody Type: Polyclonal Antibody View All» Qty/Pk: 100 µg View All» Format: Affinity Purified View All» Host: Rabbit View All»

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