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SERPINH1 antibody

The Rabbit Monoclonal anti-SERPINH1 antibody has been validated for WB, IHC and IF. It is suitable to detect SERPINH1 in samples from Human.
Catalog No. ABIN7270238

Quick Overview for SERPINH1 antibody (ABIN7270238)

Target

See all SERPINH1 Antibodies
SERPINH1 (Serpin Family H Member 1 (SERPINH1))

Reactivity

  • 66
  • 26
  • 24
  • 2
  • 2
  • 2
  • 1
  • 1
  • 1
  • 1
Human

Host

  • 51
  • 27
Rabbit

Clonality

  • 52
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Monoclonal

Conjugate

  • 43
  • 6
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  • 4
  • 4
  • 4
  • 2
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
  • 1
This SERPINH1 antibody is un-conjugated

Application

  • 59
  • 33
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  • 1
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Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Purpose

    HSP47/SERPINH1 Rabbit mAb

    Cross-Reactivity

    Human, Mouse

    Characteristics

    Monoclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthesized peptide derived from human HSP47/SERPINH1

    Isotype

    IgG
  • Application Notes

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

    SERPINH1 (Serpin Family H Member 1 (SERPINH1))

    Alternative Name

    SERPINH1

    Background

    This gene encodes a member of the serpin superfamily of serine proteinase inhibitors. The encoded protein is localized to the endoplasmic reticulum and plays a role in collagen biosynthesis as a collagen-specific molecular chaperone. Autoantibodies to the encoded protein have been found in patients with rheumatoid arthritis. Expression of this gene may be a marker for cancer, and nucleotide polymorphisms in this gene may be associated with preterm birth caused by preterm premature rupture of membranes. Alternatively spliced transcript variants have been observed for this gene, and a pseudogene of this gene is located on the short arm of chromosome 9. [provided by RefSeq, May 2011],AsTP3, CBP1, CBP2, HSP47, OI10, PIG14, PPROM, RA-A47, SERPINH2, gp46,Epigenetics & Nuclear Signaling,RNA Binding,Signal Transduction,SERPINH1

    Molecular Weight

    46kDa

    Gene ID

    871

    UniProt

    P50454
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