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SAR1B Antibody (1C7) [mFluor Violet 610 SE]

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SAR1B Antibody (1C7) [mFluor Violet 610 SE] [NBP2-22566MFV610] - Vial of mFluor Violet 610 conjugated antibody. mFluor Violet 610 is optimally excited at 421 nm by the Violet laser (405 nm) and has an emission maximum ...read more

Product Details

Summary
Reactivity HuSpecies Glossary
Applications WB, ELISA, Flow, ICC/IF
Clone
1C7
Clonality
Monoclonal
Host
Mouse
Conjugate
mFluor Violet 610 SE

Order Details

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SAR1B Antibody (1C7) [mFluor Violet 610 SE] Summary

Immunogen
Recombinant human SAR1B (1-198aa) purified from E. coli
Isotype
IgG1 Kappa
Clonality
Monoclonal
Host
Mouse
Gene
SAR1B
Purity
Protein A purified
Innovator's Reward
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Applications/Dilutions

Dilutions
  • ELISA
  • Flow Cytometry
  • Immunocytochemistry/ Immunofluorescence
  • Western Blot
Application Notes
Optimal dilution of this antibody should be experimentally determined.

Packaging, Storage & Formulations

Storage
Store at 4C in the dark.
Buffer
50mM Sodium Borate
Preservative
0.05% Sodium Azide
Purity
Protein A purified

Notes

mFluor(TM) is a trademark of AAT Bioquest, Inc. This conjugate is made on demand. Actual recovery may vary from the stated volume of this product. The volume will be greater than or equal to the unit size stated on the datasheet.

Alternate Names for SAR1B Antibody (1C7) [mFluor Violet 610 SE]

  • 2310075M17Rik
  • ANDD
  • CMRD
  • EC 3.6.5
  • GTP-binding protein B
  • GTP-binding protein SAR1b
  • GTP-binding protein Sara
  • SAR1 homolog B (S. cerevisiae)
  • SAR1a gene homolog (S. cerevisiae) 2
  • SAR1a gene homolog 2 (S. cerevisiae)
  • SAR1a gene homolog 2
  • SARA2GTBPB
  • SARB

Background

SAR1B belongs to the small GTPase superfamily, SAR1 family. It is involved in transport from the endoplasmic reticulum to the Golgi apparatus and is activated by the guanine nucleotide exchange factor PREB. SAR1B is involved in the selection of the protein cargo and the assembly of the COPII coat complex. Defects in SAR1B are the cause of chylomicron retention disease (CMRD). CMRD is an autosomal recessive disorder of severe fat malabsorption associated with failure to thrive in infancy. The conditions are characterized by deficiency of fat-soluble vitamins, low blood cholesterol levels, and a selective absence of chylomicrons from blood. Affected individuals accumulate chylomicron-like particles in membrane-bound compartments of enterocytes, which contain large cytosolic lipid droplets.

Limitations

This product is for research use only and is not approved for use in humans or in clinical diagnosis. Primary Antibodies are guaranteed for 1 year from date of receipt.

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Product General Protocols

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Video Protocols

WB Video Protocol
ICC/IF Video Protocol

FAQs for SAR1B Antibody (NBP2-22566MFV610) (0)

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Secondary Antibodies

 

Isotype Controls

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Bioinformatics

Gene Symbol SAR1B