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Image Unavailable-APOSBICL224-250MG

EMCH.HCl (E-Maleimidocaproic acid hydrazine hydrochloride)

Beskrivning: Sulphhydryl reactive -Carbohydrate reactive
Artikel nummer : APOSBICL224-250MG
UOM: 1 * 250 mg
Leverantör: Apollo Scientific
Product Image-ACRO398681000

GMBS (N-Succinimidyl 4-maleimidobutyrate) 97%

Beskrivning: GMBS (N-Succinimidyl 4-maleimidobutyrate) 97%
Artikel nummer : ACRO398681000
UOM: 1 * 100 mg
Leverantör: Thermo Fisher Scientific

Säkerhetsdatablad


Image Unavailable-TCIAM3079-50MG

Mal-amido-PEG2-NHS ≥98.0% (by GC, total nitrogen)

Beskrivning: Mal-amido-PEG2-NHS ≥98.0% (by GC, total nitrogen)
Artikel nummer : TCIAM3079-50MG
UOM: 1 * 50 mg
Leverantör: TCI
Image Unavailable-BOSSBS-9068R-CY5.5

Anti-HMBS Rabbit Polyclonal Antibody (Cy5.5®)

Beskrivning: PBGD, also designated hydroxymethylbilane synthase, is a cytoplasmic enzyme found in the heme synthesis pathway. PBGD belongs to the HMBS (hydroxymethylbilane synthase) family. Deficiency of PBGD causes errors in pyrrole metabolism, which in turn leads to an inherited autosomal disorder called acute intermittent porphyria (AIP). AIP is characterized by acute attacks of neurological dysfunctions with hypertension, tachycardia, peripheral neurologic disturbances, abdominal pain and excessive amounts of aminolevulinic acid and porphobilinogen in the urine.
Artikel nummer : BOSSBS-9068R-CY5.5
UOM: 1 * 100 µl
Leverantör: Bioss
Image Unavailable-BOSSBS-9068R-CY7

Anti-HMBS Rabbit Polyclonal Antibody (Cy7®)

Beskrivning: PBGD, also designated hydroxymethylbilane synthase, is a cytoplasmic enzyme found in the heme synthesis pathway. PBGD belongs to the HMBS (hydroxymethylbilane synthase) family. Deficiency of PBGD causes errors in pyrrole metabolism, which in turn leads to an inherited autosomal disorder called acute intermittent porphyria (AIP). AIP is characterized by acute attacks of neurological dysfunctions with hypertension, tachycardia, peripheral neurologic disturbances, abdominal pain and excessive amounts of aminolevulinic acid and porphobilinogen in the urine.
Artikel nummer : BOSSBS-9068R-CY7
UOM: 1 * 100 µl
Leverantör: Bioss
Image Unavailable-BOSSBS-9068R-A488

Anti-HMBS Rabbit Polyclonal Antibody (Alexa Fluor® 488)

Beskrivning: PBGD, also designated hydroxymethylbilane synthase, is a cytoplasmic enzyme found in the heme synthesis pathway. PBGD belongs to the HMBS (hydroxymethylbilane synthase) family. Deficiency of PBGD causes errors in pyrrole metabolism, which in turn leads to an inherited autosomal disorder called acute intermittent porphyria (AIP). AIP is characterized by acute attacks of neurological dysfunctions with hypertension, tachycardia, peripheral neurologic disturbances, abdominal pain and excessive amounts of aminolevulinic acid and porphobilinogen in the urine.
Artikel nummer : BOSSBS-9068R-A488
UOM: 1 * 100 µl
Leverantör: Bioss
Image Unavailable-BOSSBS-9068R-CY5

Anti-HMBS Rabbit Polyclonal Antibody (Cy5®)

Beskrivning: PBGD, also designated hydroxymethylbilane synthase, is a cytoplasmic enzyme found in the heme synthesis pathway. PBGD belongs to the HMBS (hydroxymethylbilane synthase) family. Deficiency of PBGD causes errors in pyrrole metabolism, which in turn leads to an inherited autosomal disorder called acute intermittent porphyria (AIP). AIP is characterized by acute attacks of neurological dysfunctions with hypertension, tachycardia, peripheral neurologic disturbances, abdominal pain and excessive amounts of aminolevulinic acid and porphobilinogen in the urine.
Artikel nummer : BOSSBS-9068R-CY5
UOM: 1 * 100 µl
Leverantör: Bioss
Image Unavailable-BOSSBS-9068R-A647

Anti-HMBS Rabbit Polyclonal Antibody (Alexa Fluor® 647)

Beskrivning: PBGD, also designated hydroxymethylbilane synthase, is a cytoplasmic enzyme found in the heme synthesis pathway. PBGD belongs to the HMBS (hydroxymethylbilane synthase) family. Deficiency of PBGD causes errors in pyrrole metabolism, which in turn leads to an inherited autosomal disorder called acute intermittent porphyria (AIP). AIP is characterized by acute attacks of neurological dysfunctions with hypertension, tachycardia, peripheral neurologic disturbances, abdominal pain and excessive amounts of aminolevulinic acid and porphobilinogen in the urine.
Artikel nummer : BOSSBS-9068R-A647
UOM: 1 * 100 µl
Leverantör: Bioss
Image Unavailable-BOSSBS-9068R-A680

Anti-HMBS Rabbit Polyclonal Antibody (Alexa Fluor® 680)

Beskrivning: PBGD, also designated hydroxymethylbilane synthase, is a cytoplasmic enzyme found in the heme synthesis pathway. PBGD belongs to the HMBS (hydroxymethylbilane synthase) family. Deficiency of PBGD causes errors in pyrrole metabolism, which in turn leads to an inherited autosomal disorder called acute intermittent porphyria (AIP). AIP is characterised by acute attacks of neurological dysfunctions with hypertension, tachycardia, peripheral neurologic disturbances, abdominal pain and excessive amounts of aminolevulinic acid and porphobilinogen in the urine.
Artikel nummer : BOSSBS-9068R-A680
UOM: 1 * 100 µl
Leverantör: Bioss
Image Unavailable-BOSSBS-9068R-A750

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

Beskrivning: PBGD, also designated hydroxymethylbilane synthase, is a cytoplasmic enzyme found in the heme synthesis pathway. PBGD belongs to the HMBS (hydroxymethylbilane synthase) family. Deficiency of PBGD causes errors in pyrrole metabolism, which in turn leads to an inherited autosomal disorder called acute intermittent porphyria (AIP). AIP is characterised by acute attacks of neurological dysfunctions with hypertension, tachycardia, peripheral neurologic disturbances, abdominal pain and excessive amounts of aminolevulinic acid and porphobilinogen in the urine.
Artikel nummer : BOSSBS-9068R-A750
UOM: 1 * 100 µl
Leverantör: Bioss
Image Unavailable-TCIAS0399-100MG

GMBS (N-Succinimidyl 4-maleimidobutyrate) ≥98.0% (by HPLC, total nitrogen) cross-linking reagent

Beskrivning: GMBS (N-Succinimidyl 4-maleimidobutyrate) ≥98.0% (by HPLC, total nitrogen) cross-linking reagent
Artikel nummer : TCIAS0399-100MG
UOM: 1 * 100 mg
Leverantör: TCI
Image Unavailable-TCIAS0398-100MG

MBS (N-Succinimidyl 3-maleimidobenzoate) ≥98.0% (by HPLC, total nitrogen) cross-linking reagent

Beskrivning: MBS (N-Succinimidyl 3-maleimidobenzoate) ≥98.0% (by HPLC, total nitrogen) cross-linking reagent
Artikel nummer : TCIAS0398-100MG
UOM: 1 * 100 mg
Leverantör: TCI
Image Unavailable-BOSSBS-9068R-FITC

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

Beskrivning: PBGD, also designated hydroxymethylbilane synthase, is a cytoplasmic enzyme found in the heme synthesis pathway. PBGD belongs to the HMBS (hydroxymethylbilane synthase) family. Deficiency of PBGD causes errors in pyrrole metabolism, which in turn leads to an inherited autosomal disorder called acute intermittent porphyria (AIP). AIP is characterized by acute attacks of neurological dysfunctions with hypertension, tachycardia, peripheral neurologic disturbances, abdominal pain and excessive amounts of aminolevulinic acid and porphobilinogen in the urine.
Artikel nummer : BOSSBS-9068R-FITC
UOM: 1 * 100 µl
Leverantör: Bioss
Image Unavailable-BOSSBS-9068R-CY3

Anti-HMBS Rabbit Polyclonal Antibody (Cy3®)

Beskrivning: PBGD, also designated hydroxymethylbilane synthase, is a cytoplasmic enzyme found in the heme synthesis pathway. PBGD belongs to the HMBS (hydroxymethylbilane synthase) family. Deficiency of PBGD causes errors in pyrrole metabolism, which in turn leads to an inherited autosomal disorder called acute intermittent porphyria (AIP). AIP is characterized by acute attacks of neurological dysfunctions with hypertension, tachycardia, peripheral neurologic disturbances, abdominal pain and excessive amounts of aminolevulinic acid and porphobilinogen in the urine.
Artikel nummer : BOSSBS-9068R-CY3
UOM: 1 * 100 µl
Leverantör: Bioss
Image Unavailable-BOSSBS-9068R

Anti-HMBS Rabbit Polyclonal Antibody

Beskrivning: PBGD, also designated hydroxymethylbilane synthase, is a cytoplasmic enzyme found in the heme synthesis pathway. PBGD belongs to the HMBS (hydroxymethylbilane synthase) family. Deficiency of PBGD causes errors in pyrrole metabolism, which in turn leads to an inherited autosomal disorder called acute intermittent porphyria (AIP). AIP is characterized by acute attacks of neurological dysfunctions with hypertension, tachycardia, peripheral neurologic disturbances, abdominal pain and excessive amounts of aminolevulinic acid and porphobilinogen in the urine.
Artikel nummer : BOSSBS-9068R
UOM: 1 * 100 µl
Leverantör: Bioss
Image Unavailable-BOSSBS-9068R-A350

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

Beskrivning: PBGD, also designated hydroxymethylbilane synthase, is a cytoplasmic enzyme found in the heme synthesis pathway. PBGD belongs to the HMBS (hydroxymethylbilane synthase) family. Deficiency of PBGD causes errors in pyrrole metabolism, which in turn leads to an inherited autosomal disorder called acute intermittent porphyria (AIP). AIP is characterized by acute attacks of neurological dysfunctions with hypertension, tachycardia, peripheral neurologic disturbances, abdominal pain and excessive amounts of aminolevulinic acid and porphobilinogen in the urine.
Artikel nummer : BOSSBS-9068R-A350
UOM: 1 * 100 µl
Leverantör: Bioss
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