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LMAN1 antibody

This anti-LMAN1 antibody is a Rabbit Monoclonal antibody detecting LMAN1 in WB and IHC. Suitable for Human.
Catalog No. ABIN7268205

Quick Overview for LMAN1 antibody (ABIN7268205)

Target

See all LMAN1 Antibodies
LMAN1 (Lectin, Mannose-Binding, 1 (LMAN1))

Reactivity

  • 41
  • 13
  • 11
  • 6
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 2
  • 1
  • 1
Human

Host

  • 39
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Rabbit

Clonality

  • 35
  • 6
Monoclonal

Conjugate

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  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This LMAN1 antibody is un-conjugated

Application

  • 36
  • 14
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  • 7
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  • 1
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Western Blotting (WB), Immunohistochemistry (IHC)
  • Purpose

    LMAN1 Rabbit mAb

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthesized peptide derived from human LMAN1

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IHC,1:50 - 1:200

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,0.05 % BSA,50 % glycerol, pH 7.3.

    Preservative

    Sodium azide

    Precaution of Use

    This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.

    Storage

    -20 °C

    Storage Comment

    Store at -20°C. Avoid freeze / thaw cycles.
  • Target

    LMAN1 (Lectin, Mannose-Binding, 1 (LMAN1))

    Alternative Name

    LMAN1

    Background

    The protein encoded by this gene is a membrane mannose-specific lectin that cycles between the endoplasmic reticulum, endoplasmic reticulum-Golgi intermediate compartment, and cis-Golgi, functioning as a cargo receptor for glycoprotein transport. The protein has an N-terminal signal sequence, a calcium-dependent and pH -sensitive carbohydrate recognition domain, a stalk region that functions in oligomerization, a transmembrane domain, and a short cytoplasmic domain required for organelle targeting. Allelic variants of this gene are associated with the autosomal recessive disorder combined factor V-factor VIII deficiency. [provided by RefSeq, Jul 2015],ERGIC-53, ERGIC53, F5F8D, FMFD1, MCFD1, MR60, gp58,Signal Transduction,LMAN1

    Molecular Weight

    58kDa

    Gene ID

    3998

    UniProt

    P49257
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