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You Searched For: Gallium+(III)+chloride


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Iron(III) chloride hexahydrate 97% ACS, Fluka™

Supplier: Honeywell Chemicals
Description: Iron(III) chloride hexahydrate 97% ACS, Fluka™

MSDS Certificates

Image Unavailable-44240.18

Indium gallium alloy (60:40 w%) ≥99.99% (metals basis)

Supplier: Thermo Fisher Scientific
Description: Indium gallium alloy (60:40 w%) ≥99.99% (metals basis)

MSDS Certificates

Product Image-HACH204253

Iron(III) chloride solution in sulphuric acid

Catalog Number: (HACH204253)
Supplier: Hach
Description: Ferric Chloride-Sulfuric Acid Solution for determination of volatile acids by the esterification method.
UOM: 1 * 1 L
Image Unavailable-12322-4X2.5L

Iron(III) chloride 45% (FeCl₃ basis) in aqueous solution, Purum, Fluka™

Catalog Number: (12322-4X2.5L)
Supplier: Honeywell Chemicals
Description: Iron(III) chloride 45% (FeCl₃ basis) in aqueous solution, Purum, Fluka™
UOM: 1 * 10 L
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Iron(III) chloride hexahydrate ≥99%, Puriss. p.a. Reag. Ph. Eur., Fluka™

Supplier: Honeywell Chemicals
Description: Iron(III) chloride hexahydrate ≥99%, Puriss. p.a. Reag. Ph. Eur., Fluka™

MSDS Certificates

Image Unavailable-ICNA0215349980

Iron(III) chloride, anhydrous, black powder

Supplier: MP Biomedicals
Description: Ferric chloride is a moderately strong Lewis acid and it is used as a catalyst in organic synthesis.

Image Unavailable-ICNA0215350090

Iron(III) chloride hexahydrate, clumpy solid

Supplier: MP Biomedicals
Description: Soluble in water, alcohol, ether, acetone; practically insoluble in ethyl acetate.

Image Unavailable-61490-500G

Lanthanum(III) chloride hydrate ≥98.5% (by titration analysis on dried basis) (~7 mol/mol H₂O)

Catalog Number: (61490-500G)
Supplier: Honeywell Chemicals
Description: Lanthanum(III) chloride hydrate ≥98.5% (by titration analysis on dried basis) (~7 mol/mol H₂O)
UOM: 1 * 500 g

MSDS


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Chromium(III) chloride hexahydrate ≥98% USP

Supplier: Spectrum Chemical
Description: Chromic Chloride, Hexahydrate, USP is intended for use as an additive to intravenous solutions for total parenteral nutrition. All Spectrum Chemical USP products are manufactured, packaged and stored under current Good Manufacturing Practices (cGMP) per 21CFR part 211 in FDA registered and inspected facilities.

Image Unavailable-ICNA0215253490

Lanthanum(III) chloride heptahydrate, clear to white crystalline powder ACS

Supplier: MP Biomedicals
Description: Calcium channel blocker.

Certificates

Image Unavailable-BOSSBS-13627R-CY3

Anti-CLCNKB Rabbit Polyclonal Antibody (Cy3®)

Catalog Number: (BOSSBS-13627R-CY3)
Supplier: Bioss
Description: The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter’s syndrome which is characterized by renal salt-wasting and low blood pressure.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13627R-CY7

Anti-CLCNKB Rabbit Polyclonal Antibody (Cy7®)

Catalog Number: (BOSSBS-13627R-CY7)
Supplier: Bioss
Description: The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter’s syndrome which is characterized by renal salt-wasting and low blood pressure.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13627R-A750

Anti-CLCNKB Rabbit Polyclonal Antibody (Alexa Fluor® 750)

Catalog Number: (BOSSBS-13627R-A750)
Supplier: Bioss
Description: The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter?s syndrome which is characterized by renal salt-wasting and low blood pressure.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13627R-FITC

Anti-CLCNKB Rabbit Polyclonal Antibody (FITC (Fluorescein Isothiocyanate))

Catalog Number: (BOSSBS-13627R-FITC)
Supplier: Bioss
Description: The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter’s syndrome which is characterized by renal salt-wasting and low blood pressure.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13627R-CY5

Anti-CLCNKB Rabbit Polyclonal Antibody (Cy5®)

Catalog Number: (BOSSBS-13627R-CY5)
Supplier: Bioss
Description: The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter’s syndrome which is characterized by renal salt-wasting and low blood pressure.
UOM: 1 * 100 µl
Image Unavailable-BOSSBS-13627R-A350

Anti-CLCNKB Rabbit Polyclonal Antibody (Alexa Fluor® 350)

Catalog Number: (BOSSBS-13627R-A350)
Supplier: Bioss
Description: The family of voltage-dependent chloride channels (CLCs) regulate cellular trafficking of chloride ions, a critical component of all living cells. CLCs regulate excitability in muscle and nerve cells, aid in organic solute transport, and maintain cellular volume. CLC-KA is a kidney-specific chloride channel that mediates transepithelial chloride transport in the thin ascending limb of the Henle loop in the inner medulla. CLC-KA plays a crucial role in urine concentration. The gene encoding human CLC-KA maps to chromosome 1p36. Mutations in this gene may be associated with nephrogenic diabetes insipidus in those cases where mutations in the vasopressin V2 receptor and the AQP2 water channel are lacking. CLC-KB mediates basolateral chloride ion efflux in the thick ascending limb and in more distal nephron segments. The gene encoding human CLC-KB maps to chromosome 1p36. Mutations in this gene cause type III Barter’s syndrome which is characterized by renal salt-wasting and low blood pressure.
UOM: 1 * 100 µl
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Stock for this item is limited, but may be available in a warehouse close to you. Please make sure that you are logged in to the site so that available stock can be displayed. If the call is still displayed and you need assistance, please call us on +353 1 88 22222.
This product is marked as restricted and can only be purchased by approved Shipping Accounts. If you need further assistance, email VWR Regulatory Department at eurega_services@eu.vwr.com
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