Skip to Content
Merck

H9658

Monoclonal Anti-HA antibody produced in mouse

clone HA-7, ascites fluid

Synonym(s):

Monoclonal Anti-HA, HA Antibody - Monoclonal Anti-HA antibody produced in mouse, Ha Antibody Sigma, Sigma Ha Antibody, Anti-HA, Anti-Influenza Hemagglutinin

Sign In to View Organizational & Contract Pricing.

Select a Size

100 μL

CZK 12,500.00

0.2 ML

CZK 16,600.00

CZK 12,500.00


Please contact Customer Service for Availability

Request a Bulk Order

About This Item

UNSPSC Code:
12352203
NACRES:
NA.43
MDL number:

Skip To

Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

Monoclonal Anti-HA antibody produced in mouse, clone HA-7, ascites fluid

biological source

mouse

conjugate

unconjugated

antibody form

ascites fluid

antibody product type

primary antibodies

clone

HA-7, monoclonal

contains

15 mM sodium azide

technique(s)

immunocytochemistry: suitable
immunoprecipitation (IP): suitable
indirect ELISA: suitable
western blot: 1:20,000 using extracts from 293T (human embryonic kidney) cells expressing a recombinant HA-fusion protein

isotype

IgG1

shipped in

dry ice

storage temp.

−20°C

target post-translational modification

unmodified

Quality Level

Looking for similar products? Visit Product Comparison Guide

Compare Similar Items

View Full Comparison

Show Differences

1 of 4

This Item
H3663A2095H6533
clone

HA-7, monoclonal

clone

HA-7, monoclonal

clone

HA-7, monoclonal

clone

HA-7, monoclonal

conjugate

unconjugated

conjugate

unconjugated

conjugate

agarose conjugate

conjugate

peroxidase conjugate

antibody form

ascites fluid

antibody form

purified immunoglobulin

antibody form

purified immunoglobulin

antibody form

purified from hybridoma cell culture

biological source

mouse

biological source

mouse

biological source

mouse

biological source

mouse

isotype

IgG1

isotype

IgG1

isotype

IgG1

isotype

-

technique(s)

immunocytochemistry: suitable, indirect ELISA: suitable, immunoprecipitation (IP): suitable, western blot: 1:20,000 using extracts from 293T (human embryonic kidney) cells expressing a recombinant HA-fusion protein

technique(s)

immunocytochemistry: 1.0-2.0 μg/mL, immunoprecipitation (IP): 0.5-2.0 μg, western blot: 0.25-1 μg/mL

technique(s)

-

technique(s)

western blot: 1:4,000 using using HA tagged fusion protein expressed in bacteria, and ECL immunoblotting detection reagent

Application

Monoclonal Anti-HA antibody produced in mouse has been used in 293T cells for:
  • immunoprecipitation in human embryonic kidney 293 cells
  • immunoblotting in HeLa cells
  • immunopurification in human embryonic kidney 293 cells
  • immunostaining for electron microscopy in mouse embryonic fibroblasts
  • in immunocytochemistry of hippocampal slices
Monoclonal Anti-HA antibody produced in mouse has been used in:
  • Immunoblotting, to study the expression of fusion protein
  • Coimmunoprecipitation assay
  • Immunoblotting of lysate protein

Biochem/physiol Actions

Hemagglutinin (HA) is the surface glycoprotein of influenza virus. HA is crucial for virus entry and interaction with N-acetylneuraminic acid (Neu5Ac) in host cell surface. HA coordinates with neuraminidase (NA) and facilitates viral entry into host. HA exists as a trimer and each monomer has stalk transmembrane and globular regions. The globular region contains carbohydrate side chains crucial for infecting host.
Influenza virus hemagglutinin (HA) acts as a key immunogen in avian influenza virus (AIV) vaccines. Activated HA facilitates virus attachment to oligosaccharide receptors on host cell surface and is involved in penetration through fusion following conformational modifications in the endolysosomal compartment. 226 and 228 residues in hemagglutinin (HA) of the H3 subtype play a key role in host range restriction and receptor specificity. Influenza virus hemagglutinin (HA) is responsible for 1918 influenza pandemic.
The antibody recognizes native as well as denatured-reduced forms of HA-tagged proteins and is reactive with N- or C-terminal HA-tagged fusion proteins expressed in E. coli or in mammalian cells.

Disclaimer

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.

General description

The gene encoding influenza virus hemagglutinin (HA) precursor is mapped on segment 4. It encodes a 76kDa surface glycoprotein which exists as trimers on the viral envelope.

Immunogen

synthetic peptide corresponding to a fragment of human influenza virus hemagglutinin (HA) known as HA-tag, conjugated to KLH

Preparation Note

For continuous use, store at 2-8 °C for up to one month.
For extended storage, freeze in working aliquots. Repeated freezing and thawing, or storage in "frost-free" freezers, is not recommended. If slight turbidity occurs upon prolonged storage, clarify the solution by centrifugation before use. Solutions at working dilution should be discarded if not used within 12 hours.

Not finding the right product?  

Try our Product Selector Tool.

Storage Class

12 - Non Combustible Liquids

wgk

nwg

flash_point_f

Not applicable

flash_point_c

Not applicable


Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Calmodulin shuttling mediates cytonuclear signaling to trigger experience-dependent transcription and memory
Cohen SM, et al.
Nature Communications, 9(1), 2451-2451 (2018)
Functional mutations in mouse norepinephrine transporter reduce sensitivity to cocaine inhibition.
Wei H, et al.
Neuropharmacology, 56(2), 399-404 (2009)
SIRT 5-mediated deacetylation of LDHB promotes autophagy and tumourigenesis in colorectal cancer
Shi L, et al.
Molecular Oncology (2018)
A single amino acid substitution in 1918 influenza virus hemagglutinin changes receptor binding specificity.
Glaser L, et al.
Journal of Virology, 79(17), 11533-11536 (2005)
Characterization of a novel influenza A virus hemagglutinin subtype (H16) obtained from black-headed gulls.
Fouchier R A M, et al.
Journal of Virology, 79(5), 2814-2822 (2005)

Related Content

Instructions

Questions

1–4 of 4 Questions  
  1. I want to do an IP using this HA antibody. I know it is produced in mouse but what kind of IgG is it?

    1 answer
    1. This antibody is an IgG1 isotype. Please see the link below to review additional information available in the product datasheet:_x000D_
      https://www.sigmaaldrich.com/US/en/product/sigma/h9658

      Helpful?

  2. What is the isotype and light chain for Monoclonal Anti-HA antibody clone HA-7 produced in mouse?

    1 answer
    1. Monoclonal Anti-HA antibody clone HA-7 is mouse IgG1, kappa light chain.

      Helpful?

  3. What is the Department of Transportation shipping information for this product?

    1 answer
    1. Transportation information can be found in Section 14 of the product's (M)SDS.To access the shipping information for this material, use the link on the product detail page for the product.

      Helpful?

  4. What is the recommended dilution of Product H9658 - HA antibody for immunoprecipitation and for indirect immunostaining?

    1 answer
    1. H9658 - Monoclonal Anti-HA antibody produced in mouse is the ascites fluid. It is not purified. We only test this product in western blotting.  This product contains 15-55 mg/ml total protein with 4-7 mg/ml specific antibody. H3663 - Monoclonal Anti-HA antibody produced in mouse as the purified immunoglobulin. We test this product for immunoprecipitation using 0.5-2.0 μg and for immunocytochemistry using 1.0-2.0 μg/mL.These ranges would be a good starting concentration. In order to obtain best results in different techniques and preparations, we recommend determining optimal working dilution by titration test.

      Helpful?

Reviews

No rating value

Active Filters

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service