PIPA5116705

NDUFB1 Polyclonal Antibody, Invitrogen™

Manufacturer: Thermo Scientific

Select a Size

Pack Size SKU Availability Price
Each of 1 PIPA5116705-Each-of-1 In Stock ₹ 46,502.50

PIPA5116705 - Each of 1

₹ 46,502.50

In Stock

Quantity

1

Base Price: ₹ 46,502.50

GST (18%): ₹ 8,370.45

Total Price: ₹ 54,872.95

Antigen

NDUFB1

Classification

Polyclonal

Conjugate

Unconjugated

Gene

NDUFB1

Gene Alias

CI-MNLL; CI-SGDH; complex I MNLL subunit; complex I-MNLL; MNLL; NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 1; NADH dehydrogenase (ubiquinone) 1 beta subcomplex, 1, 7kDa; NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 1; NADH:ubiquinone oxidoreductase subunit B1; NADH-ubiquinone oxidoreductase MNLL subunit; Ndufb1

Host Species

Rabbit

Purification Method

Affinity chromatography

Regulatory Status

RUO

Gene ID (Entrez)

110324555, 4707

Content And Storage

-20° C, Avoid Freeze/Thaw Cycles

Form

Liquid

Applications

Immunocytochemistry, Western Blot

Concentration

1.98 mg/mL

Formulation

PBS with 50% glycerol and 0.01% thimerosal; pH 7.3

Gene Accession No.

O75438, P0DN34

Gene Symbols

NDUFB1

Immunogen

Recombinant fusion protein containing a sequence corresponding to amino acids 1-105 of human NDUFB1 (NP_0045362)

Quantity

100 μL

Primary or Secondary

Primary

Target Species

Human, Mouse

Product Type

Antibody

Isotype

IgG

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Description

  • Positive Samples: 293T, A375, Mouse brain, Mouse pancreas Immunogen sequence: MICWRHPSAP CGRGEWQVPR SQLPLARVEF PVALGLGVAV GAEAAAIMVN LLQIVRDHWV HVLVPMGFVI GCYLDRKSDE RLTAFRNKSM LFKRELQPSE EVTWK NDUFB1 (NADH dehydrogenase [ubiquinone] 1 beta subcomplex subunit 1), also known as CI-MNLL (complex I-MNLL), CI-SGDH or NADH-ubiquinone oxidoreductase MNLL subunit, is a 58 amino acid single-pass membrane protein that localizes to the matrix side of the mitochondrial membrane
  • A member of the complex I NDUFB1 subunit family, NDUFB1 is encoded by a gene that maps to human chromosome 14q32.12
  • Chromosome 14 houses over 700 genes and comprises nearly 3.5% of the human genome
  • Chromosome 14 encodes the presinilin 1 (PSEN1) gene, which is one of the three key genes associated with the development of Alzheimer's disease (AD)
  • The SERPINA1 gene is also located on chromosome 14 and, when defective, leads to the genetic disorder alpha1-antitrypsin deficiency, which is characterized by severe lung complications and liver dysfunction.