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SAR1B antibody

The Rabbit Polyclonal anti-SAR1B antibody has been validated for WB, IHC (p), ICC and IF. It is suitable to detect SAR1B in samples from Human.
Catalog No. ABIN7468921

Quick Overview for SAR1B antibody (ABIN7468921)

Target

See all SAR1B Antibodies
SAR1B (SAR1 Homolog B (SAR1B))

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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This SAR1B antibody is un-conjugated

Application

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Western Blotting (WB), Immunohistochemistry (Paraffin-embedded Sections) (IHC (p)), Immunocytochemistry (ICC), Immunofluorescence (IF)
  • Cross-Reactivity

    Human, Mouse, Rat

    Purification

    Purified by antigen-affinity chromatography.

    Immunogen

    Full length human SAR1B Recombinant protein.

    Isotype

    IgG
  • Application Notes

    WB: 1:500-1:3000. ICC/IF: 1:100-1:1000. IHC-P: 1:100-1:1000. Optimal dilutions/concentrations should be determined by the researcher. Not tested in other applications.

    Comment

    Positive Control: Mouse brain , rat brain , HeLa

    Restrictions

    For Research Use only
  • Format

    Liquid

    Concentration

    1 mg/mL

    Buffer

    0.1M Tris-Glycine ( pH 7), 10 % Glycerol, 0.01 % Thimerosal

    Preservative

    Thimerosal (Merthiolate)

    Precaution of Use

    This product contains Thimerosal (Merthiolate): a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    4 °C,-20 °C

    Storage Comment

    Store as concentrated solution. Centrifuge briefly prior to opening vial. For short-term storage (1-2 weeks), store at 4°C. For long-term storage, aliquot and store at -20°C or below. Avoid multiple freeze-thaw cycles.
  • Target

    SAR1B (SAR1 Homolog B (SAR1B))

    Alternative Name

    secretion associated Ras related GTPase 1B

    Background

    Synonyms: secretion associated Ras related GTPase 1B , ANDD , CMRD , GTBPB , SARA2

    Background: The protein encoded by this gene is a small GTPase that acts as a homodimer. The encoded protein is activated by the guanine nucleotide exchange factor PREB and is involved in protein transport from the endoplasmic reticulum to the Golgi. This protein is part of the COPII coat complex. Defects in this gene are a cause of chylomicron retention disease (CMRD), also known as Anderson disease (ANDD). Two transcript variants encoding the same protein have been found for this gene. [provided by RefSeq]

    Molecular Weight

    22 kDa

    Gene ID

    51128

    UniProt

    Q9Y6B6

    Pathways

    Lipid Metabolism
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