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Kelch-like protein 41 (KLHL41) (AA 1-300) antibody

The Rabbit Polyclonal anti- antibody has been validated for WB. It is suitable to detect in samples from Human.
Catalog No. ABIN7268084

Quick Overview for Kelch-like protein 41 (KLHL41) (AA 1-300) antibody (ABIN7268084)

Target

See all Kelch-like protein 41 (KLHL41) Antibodies
Kelch-like protein 41 (KLHL41)

Reactivity

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Human

Host

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Rabbit

Clonality

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Polyclonal

Conjugate

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  • 1
Un-conjugated

Application

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Western Blotting (WB)
  • Binding Specificity

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    AA 1-300

    Purpose

    KLHL41 Rabbit pAb

    Sequence

    MDSQRELAEE LRLYQSTLLQ DGLKDLLDEK KFIDCTLKAG DKSLPCHRLI LSACSPYFRE YFLSEIDEAK KKEVVLDNVD PAILDLIIKY LYSASIDLND GNVQDIFALA SRFQIPSVFT VCVSYLQKRL APGNCLAILR LGLLLDCPRL AISAREFVSD RFVQICKEED FMQLSPQELI SVISNDSLNV EKEEAVFEAV MKWVRTDKEN RVKNLSEVFD CIRFRLMTEK YFKDHVEKDD IIKSNPDLQK KIKVLKDAFA GKLPEPSKNA AKTGAGEVNG DVGDEDLLPG YLNDIPRHGM

    Cross-Reactivity

    Human, Mouse, Rat

    Characteristics

    Polyclonal Antibodies

    Purification

    Affinity purification

    Immunogen

    Recombinant fusion protein containing a sequence corresponding to amino acids 1-300 of human KLHL41 (NP_006054.2).

    Isotype

    IgG
  • Application Notes

    WB,1:200 - 1:2000

    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

    Kelch-like protein 41 (KLHL41)

    Alternative Name

    KLHL41

    Background

    This gene is a member of the kelch-like family. The encoded protein contains a BACK domain, a BTB/POZ domain, and 5 Kelch repeats. This protein is thought to function in skeletal muscle development and maintenance. Mutations in this gene have been associated with nemaline myopathy (NM), a rare congenital muscle disorder.,KLHL41,KBTBD10,Krp1,SARCOSIN,Cell Biology & Developmental Biology,Ubiquitin,KLHL41

    Molecular Weight

    66kDa/68kDa

    Gene ID

    10324

    UniProt

    O60662
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