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FGD1 antibody (AA 700-800)

This anti-FGD1 antibody is a Rabbit Polyclonal antibody detecting FGD1 in WB, IHC and IF. Suitable for Human.
Catalog No. ABIN7267284

Quick Overview for FGD1 antibody (AA 700-800) (ABIN7267284)

Target

See all FGD1 Antibodies
FGD1 (FYVE, RhoGEF and PH Domain Containing 1 (FGD1))

Reactivity

  • 9
  • 5
  • 4
  • 3
  • 3
  • 2
  • 2
  • 1
Human

Host

  • 9
Rabbit

Clonality

  • 9
Polyclonal

Conjugate

  • 9
This FGD1 antibody is un-conjugated

Application

  • 8
  • 1
  • 1
  • 1
  • 1
Western Blotting (WB), Immunohistochemistry (IHC), Immunofluorescence (IF)
  • Binding Specificity

    • 4
    • 3
    • 1
    AA 700-800

    Purpose

    FGD1 Rabbit pAb

    Sequence

    LLNSTNREDE DTPPNSPNVD LGKRAPTPIR EKEVTMCMRC QEPFNSITKR RHHCKACGHV VCGKCSEFRA RLVYDNNRSN RVCTDCYVAL HGVPGSSPAC S

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    A synthetic peptide corresponding to a sequence within amino acids 700-800 of human FGD1 (NP_004454.2).

    Isotype

    IgG
  • Application Notes

    WB,1:500 - 1:2000,IHC,1:50 - 1:100,IF,1:50 - 1:100

    Restrictions

    For Research Use only
  • Format

    Liquid

    Buffer

    PBS with 0.02 % sodium azide,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

    FGD1 (FYVE, RhoGEF and PH Domain Containing 1 (FGD1))

    Alternative Name

    FGD1

    Background

    This gene encodes a protein that contains Dbl (DH) and pleckstrin (PH) homology domains and is similar to the Rho family of small GTP-binding proteins. The encoded protein specifically binds to the Rho family GTPase Cdc42Hs and can stimulate the GDP-GTP exchange of the isoprenylated form of Cdc42Hs. It also stimulates the mitogen activated protein kinase cascade leading to c-Jun kinase SAPK/JNK1 activation. Defects in this gene are the cause of faciogenital dysplasia and X-linked mental retardation, syndromatic 16.,FGD1,AAS,FGDY,MRXS16,ZFYVE3,FYVE,Signal Transduction,G protein signaling,G-Protein-Coupled Receptors(GPCR),Cell Biology & Developmental Biology,Cytoskeleton,Microfilaments,FGD1

    Molecular Weight

    106kDa

    Gene ID

    2245

    UniProt

    P98174

    Pathways

    Neurotrophin Signaling Pathway
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