MABN821MI

MilliporeSigma™ polyQ Disease Proteins, Mouse, Unlabeled, Clone: 3B5H10,

Manufacturer: MilliporeSigma™

Select a Size

Pack Size SKU Availability Price
Each of 1 MABN821MI-Each-of-1 In Stock ₹ 39,152.26

MABN821MI - Each of 1

₹ 39,152.26

In Stock

Quantity

1

Base Price: ₹ 39,152.26

GST (18%): ₹ 7,047.407

Total Price: ₹ 46,199.667

Antigen

polyQ Disease Proteins

Classification

Monoclonal

Concentration

Please refer to lot specific datasheet.

Formulation

Purified mouse IgG1 in buffer containing 0.1M Tris-Glycine (pH 7.4), 150mM NaCl with 0.05% Sodium Azide.

Gene Accession No.

P42858

Immunogen

N-terminally GST-tagged human Huntingtin (Htt) fragment corresponding to exon 1-coded seqeunce containing a stretch of 66 glutamines (GST-171-Q66; Miller, J., et al. (2011). Nat. Chem. Biol. 7(12):925-934).

Quantity

100 μg

Research Discipline

Neuroscience

Test Specificity

Clone 3B5H10 targeted epitope is exposed among some of the many conformations adopted by monomeric and possibly small oligomeric polyQ species of mutant Huntingtin protein (mHtt), but disappears in higher-molecular weight aggregated forms, such as inclusion bodies (IBs). The epitope also exists in mutant forms of other polyQ-containing proteins that cause neurodegeneration, including the androgen receptor, atrophin, and ataxin-3 (Miller, J., et al. (2011). Nat. Chem. Biol. 7(12):925-934).

Content And Storage

Stable for 1 year at 2°-8°C from date of receipt.

Isotype

IgG1

Applications

Immunocytochemistry, Immunohistochemistry, Inhibition Assays, Western Blot

Clone

3B5H10

Conjugate

Unconjugated

Gene

HTT, HD, IT15

Host Species

Mouse

Purification Method

Protein G Purified

Regulatory Status

RUO

Primary or Secondary

Primary

Target Species

Human

Form

Purified

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Description

  • Huntingtin (UniProt P42858; also known as HD protein, Huntington disease protein) is encoded by the HTT (also known as HD, IT15) gene (Gene ID 3064) in human
  • Misfolding and self-aggregation of specific proteins are a common feature of well known neurodegenerative diseases, including Huntington s disease (HD), Alzheimer's disease (AD), Parkinson s disease (PD), and amyotrophic lateral sclerosis (AML)
  • Abnormal polyglutamine (polyQ) repeat sequence or stretch result in protein misfolding and neurodegeneration
  • HD, for example, is caused by polyQ expansion in the first exon-coded sequence of the causal protein Huntingtin (Htt exon 1)
  • The expanded polyQ leads to formation of beta-sheet rich fibrillar aggregates called amyloid
  • Eight proteins containing polyQ tracts, but otherwise unrelated to htt, also result in protein misfolding and neurodegeneration upon polyQ expansion
  • Growing evidences implicate soluble oligomers or even monomers of disease-causing amyloid proteins as the more toxic species
  • In HD, formation of the end-stage, very large aggregated species of mutant htt (mHtt), termed an inclusion bodies (IBs), is believed to be a coping response to sequester toxic species of monomeric or small oligomeric mHtt, which are distributed diffusely throughout the neuron.

Compare Similar Items

Show Difference

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MilliporeSigma™

MABN821MI

--


Antigen:
polyQ Disease Proteins

Classification:
Monoclonal

Concentration:
Please refer to lot specific datasheet.

Formulation:
Purified mouse IgG1 in buffer containing 0.1M Tris-Glycine (pH 7.4), 150mM NaCl with 0.05% Sodium Azide.

Gene Accession No.:
P42858

Immunogen:
N-terminally GST-tagged human Huntingtin (Htt) fragment corresponding to exon 1-coded seqeunce containing a stretch of 66 glutamines (GST-171-Q66; Miller, J., et al. (2011). Nat. Chem. Biol. 7(12):925-934).

Quantity:
100 μg

Research Discipline:
Neuroscience

Test Specificity:
Clone 3B5H10 targeted epitope is exposed among some of the many conformations adopted by monomeric and possibly small oligomeric polyQ species of mutant Huntingtin protein (mHtt), but disappears in higher-molecular weight aggregated forms, such as inclusion bodies (IBs). The epitope also exists in mutant forms of other polyQ-containing proteins that cause neurodegeneration, including the androgen receptor, atrophin, and ataxin-3 (Miller, J., et al. (2011). Nat. Chem. Biol. 7(12):925-934).

Content And Storage:
Stable for 1 year at 2°-8°C from date of receipt.

Isotype:
IgG1

Applications:
Immunocytochemistry, Immunohistochemistry, Inhibition Assays, Western Blot

Clone:
3B5H10

Conjugate:
Unconjugated

Gene:
HTT, HD, IT15

Host Species:
Mouse

Purification Method:
Protein G Purified

Regulatory Status:
RUO

Primary or Secondary:
Primary

Target Species:
Human

Form:
Purified

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MABN828MI

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Antigen:
LRRTM4

Classification:
Monoclonal

Concentration:
__

Formulation:
Purified mouse monoclonal IgG1κ in buffer containing 0.1M Tris-Glycine (pH 7.4), 150mM NaCl with 0.05% sodium azide.

Gene Accession No.:
Q86VH4

Immunogen:
Conjugated linear peptide corresponding to human LRRTM4.

Quantity:
100 μg

Research Discipline:
Neuroscience

Test Specificity:
__

Content And Storage:
Stable for one year at 2°C to 8°C from date of receipt.

Isotype:
IgG1 κ

Applications:
Immunocytochemistry, Immunohistochemistry, Western Blot

Clone:
N205B/22

Conjugate:
__

Gene:
__

Host Species:
Mouse

Purification Method:
Protein G Purified

Regulatory Status:
RUO

Primary or Secondary:
Primary

Target Species:
Human, Mouse, Rat

Form:
Purified

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MABN838MI

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Antigen:
Retinal Dehydrogenase 1/ALDH1A1

Classification:
Monoclonal

Concentration:
__

Formulation:
Purified mouse monoclonal IgG1k antibody in buffer containing 0.1M Tris-Glycine (pH 7.4), 150mM NaCl with 0.05% sodium azide.

Gene Accession No.:
P00352

Immunogen:
GST-tagged recombinant protein corresponding to the N-terminal of human Retinal Dehydrogenase 1/ALDH1A1.

Quantity:
100 μg

Research Discipline:
Neuroscience

Test Specificity:
__

Content And Storage:
2°C to 8°C for one year from date of shipment

Isotype:
IgG1 κ

Applications:
Immunohistochemistry (Paraffin), Western Blot

Clone:
8D7.1

Conjugate:
Unconjugated

Gene:
__

Host Species:
Mouse

Purification Method:
Protein G purified

Regulatory Status:
RUO

Primary or Secondary:
Primary

Target Species:
Human

Form:
Purified

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Antigen:
Semaphorin 4A

Classification:
Monoclonal

Concentration:
__

Formulation:
Purified mouse monoclonal IgMκ antibody in PBS with 0.05% sodium azide.

Gene Accession No.:
Q9H3S1

Immunogen:
GST-tagged recombinant protein corresponding to the Sema domain of human Semaphorin 4A.

Quantity:
100 μg

Research Discipline:
Neuroscience

Test Specificity:
__

Content And Storage:
Stable for one year at 2°C to 8°C from date of receipt.

Isotype:
IgM κ

Applications:
Western Blot

Clone:
8B5.1

Conjugate:
__

Gene:
__

Host Species:
Mouse

Purification Method:
Purified by Ion-Exchange Chromatography

Regulatory Status:
RUO

Primary or Secondary:
Primary

Target Species:
Human

Form:
Purified